14 results on '"Hipp, Stephanie"'
Search Results
2. Artificial vision with wirelessly powered subretinal electronic implant alpha-IMS
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Stingl, Katarina, Bartz-Schmidt, Karl Ulrich, Besch, Dorothea, Braun, Angelika, Bruckmann, Anna, Gekeler, Florian, Greppmaier, Udo, Hipp, Stephanie, Hörtdörfer, Gernot, Kernstock, Christoph, Koitschev, Assen, Kusnyerik, Akos, Sachs, Helmut, Schatz, Andreas, Stingl, Krunoslav T., Peters, Tobias, Wilhelm, Barbara, and Zrenner, Eberhart
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- 2013
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3. Phenotype variations of retinal dystrophies caused by mutations in the RLBP1 gene
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Hipp, Stephanie, Zobor, Gergely, Glöckle, Nicola, Mohr, Julia, Kohl, Susanne, Zrenner, Eberhart, Weisschuh, Nicole, and Zobor, Ditta
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- 2015
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4. Usher Syndrome and Color Vision
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Kurtenbach, Anne, primary, Hahn, Gesa, additional, Kernstock, Christoph, additional, Hipp, Stephanie, additional, Zobor, Ditta, additional, Stingl, Katarina, additional, Kohl, Susanne, additional, Bonnet, Crystel, additional, Mohand-Saïd, Saddek, additional, Sliesoraityte, Ieva, additional, Sahel, José-Alain, additional, Audo, Isabelle, additional, Fakin, Ana, additional, Hawlina, Marko, additional, Testa, Francesco, additional, Simonelli, Francesca, additional, Petit, Christine, additional, and Zrenner, Eberhart, additional
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- 2018
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5. Phenotype Variations Caused by Mutations in theRP1L1Gene in a Large Mainly German Cohort
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Zobor, Ditta, primary, Zobor, Gergely, additional, Hipp, Stephanie, additional, Baumann, Britta, additional, Weisschuh, Nicole, additional, Biskup, Saskia, additional, Sliesoraityte, Ieva, additional, Zrenner, Eberhart, additional, and Kohl, Susanne, additional
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- 2018
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6. Home-Based Comprehensive Medication Reviews: Pharmacist's Impact on Drug Therapy Problems in Geriatric Patients
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Steele, Katelyn M., primary, Ruisinger, Janelle F., additional, Bates, Jessica, additional, Prohaska, Emily S., additional, Melton, Brittany L., additional, and Hipp, Stephanie, additional
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- 2016
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7. Mutations in C8orf37, Encoding a Ciliary Protein, are Associated with Autosomal-Recessive Retinal Dystrophies with Early Macular Involvement
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Estrada-Cuzcano, Alejandro, Neveling, Kornelia, Kohl, Susanne, Banin, Eyal, Rotenstreich, Ygal, Sharon, Dror, Falik-Zaccai, Tzipora C., Hipp, Stephanie, Roepman, Ronald, Wissinger, Bernd, Letteboer, Stef J.F., Mans, Dorus A., Blokland, Ellen A.W., Kwint, Michael P., Gijsen, Sabine J., van Huet, Ramon A.C., Collin, Rob W.J., Scheffer, H., Veltman, Joris A., Zrenner, Eberhart, den Hollander, Anneke I., Klevering, B. Jeroen, and Cremers, Frans P.M.
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- 2012
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8. Morphometric Optic Nerve Head Analysis in Glaucoma Patients: A Comparison between the Simultaneous Nonmydriatic Stereoscopic Fundus Camera (Kowa Nonmyd WX3D) and the Heidelberg Scanning Laser Ophthalmoscope (HRT III)
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Mariacher, Siegfried, primary, Hipp, Stephanie, additional, Wirthky, Robert, additional, Blumenstock, Gunnar, additional, Bartz-Schmidt, Karl-Ulrich, additional, Ziemssen, Focke, additional, Schiefer, Ulrich, additional, Voykov, Bogomil, additional, and Januschowski, Kai, additional
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- 2016
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9. Phenotype variations of retinal dystrophies caused by mutations in theRLBP1gene
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Hipp, Stephanie, primary, Zobor, Gergely, additional, Glöckle, Nicola, additional, Mohr, Julia, additional, Kohl, Susanne, additional, Zrenner, Eberhart, additional, Weisschuh, Nicole, additional, and Zobor, Ditta, additional
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- 2014
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10. Cell surface engineering using glycosylphosphatidylinositol anchored tissue inhibitor of matrix metalloproteinase-1 stimulates cutaneous wound healing
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Djafarzadeh, Roghieh, primary, Conrad, Claudius, additional, Notohamiprodjo, Susan, additional, Hipp, Stephanie, additional, Niess, Hanno, additional, Bruns, Christiane J., additional, and Nelson, Peter J., additional
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- 2014
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11. Clinical Characteristics of Rod and Cone Photoreceptor Dystrophies in Patients With Mutations in theC8orf37Gene
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van Huet, Ramon A. C., primary, Estrada-Cuzcano, Alejandro, additional, Banin, Eyal, additional, Rotenstreich, Ygal, additional, Hipp, Stephanie, additional, Kohl, Susanne, additional, Hoyng, Carel B., additional, den Hollander, Anneke I., additional, Collin, Rob W. J., additional, and Klevering, B. Jeroen, additional
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- 2013
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12. Full-field electroretinography, visual acuity and visual fields in Usher syndrome: a multicentre European study
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Christoph Kernstock, Ditta Zobor, Anne Kurtenbach, Francesca Simonelli, Susanne Kohl, Stephanie Hipp, José-Alain Sahel, Marko Hawlina, Isabelle Audo, Saddek Mohand-Said, Crystel Bonnet, Christine Petit, Eberhart Zrenner, Katarina Stingl, Gesa Hahn, Francesco Testa, Ana Fakin, Institute for Ophthalmic Research [Tübingen, Germany] (Centre for Ophthalmology), University of Tübingen, University of Tuebingen, Génétique et Physiologie de l'Audition, Institut Pasteur [Paris] (IP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU), Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts (CHNO), Institut de la Vision, Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), University Medical Centre Ljubljana [Ljubljana, Slovenia] (UMCL), University of the Study of Campania Luigi Vanvitelli, Collège de France - Chaire Génétique et physiologie cellulaire, Collège de France (CdF (institution)), Fondation Ophtalmologique Adolphe de Rothschild [Paris], University of Pittsburgh School of Medicine, Pennsylvania Commonwealth System of Higher Education (PCSHE), Tuebingen University [Germany], This work was supported by the European Union Seventh Framework Programme under the Grant Agreement HEALTH-F2-2010-242013 (TREATRUSH) and the Tistou and Charlotte Kerstan Foundation., European Project: 242013,EC:FP7:HEALTH,FP7-HEALTH-2009-single-stage,TREATRUSH(2010), Institut Pasteur [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU), Centre National de la Recherche Scientifique (CNRS)-Sorbonne Université (SU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Chaire Génétique et physiologie cellulaire, Stingl, Katarina, Kurtenbach, Anne, Hahn, Gesa, Kernstock, Christoph, Hipp, Stephanie, Zobor, Ditta, Kohl, Susanne, Bonnet, Crystel, Mohand-Said, Saddek, Audo, Isabelle, Fakin, Ana, Hawlina, Marko, Testa, Francesco, Simonelli, Francesca, Petit, Christine, Sahel, Jose-Alain, and Zrenner, Eberhart
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Male ,Visual acuity ,genetic structures ,Usher syndrome ,[SDV]Life Sciences [q-bio] ,Visual Acuity ,MESH: Electroretinography ,MESH: Visual Acuity ,0302 clinical medicine ,Functional diagnostics ,MESH: Middle Aged ,medicine.diagnostic_test ,MESH: Visual Field Tests ,MESH: Retina ,MESH: European Continental Ancestry Group ,Middle Aged ,Visual field ,Sensory Systems ,Phenotype ,MESH: Young Adult ,ERG ,Female ,medicine.symptom ,Erg ,Usher Syndromes ,Retinitis Pigmentosa ,Photopic vision ,Adult ,medicine.medical_specialty ,Context (language use) ,MESH: Phenotype ,Retina ,White People ,03 medical and health sciences ,Young Adult ,Physiology (medical) ,Ophthalmology ,Retinitis pigmentosa ,medicine ,otorhinolaryngologic diseases ,Electroretinography ,Humans ,MESH: Usher Syndromes ,MESH: Humans ,business.industry ,MESH: Adult ,Functional diagnostic ,medicine.disease ,eye diseases ,MESH: Male ,030221 ophthalmology & optometry ,MESH: Retinitis Pigmentosa ,Visual Field Tests ,MESH: Visual Fields ,Visual Fields ,business ,MESH: Female ,030217 neurology & neurosurgery - Abstract
Purpose: Usher syndrome (USH) is a multisensory deficiency involving vision, hearing and the vestibular system. The purpose of this study is to report on the functional data (i.e. electroretinography, visual fields, visual acuity) of patients with retinitis pigmentosa (RP) due to Usher syndrome that were collected in a multicentre European study (TREATRUSH). Methods: A total of 268 genetically confirmed USH patients underwent electrophysiological examinations in the context of multimodal ophthalmological examination in the study (75 USH1, 189 USH2 and four USH3). Full-field electroretinography (ERG) was performed according to ISCEV standards, visual field determination was carried out with either the Octopus or Goldmann perimeters and visual acuity was examined with either ETDRS or Snellen charts. The data were compared between USH subtypes (USH1/USH2/USH3) and correlated with age. Results: Visual acuity decreases significantly with age for both USH1 and USH2 (p < 0.001), without a difference between the two cohorts. When corrected for age, the preserved kinetic visual field was significantly larger in USH2 than in USH1 (p = 0.04). Furthermore, the preserved kinetic visual field area showed a significant decrease with age (based on an exponential fit) in both USH1 and USH2 (p < 0.001). In USH1 patients, however, the visual field was already vastly reduced at an early age. The ERG results were abnormal in all patients. Detectable data for scotopic ERG were obtained from nine patients, and data of photopic ERG were obtained from 24 patients, without a difference between USH1 and USH2 subtypes. Conclusions: There are differences in the phenotypes of RP in USH subtypes, most visible in the progression of visual fields between USH1 and USH2. The perimetric reduction occurs earlier in USH1 than in USH2. In both subtypes, visual acuity decreases significantly with age and the ERG is not detectable already at early ages. Purpose: Usher syndrome (USH) is a multisensory deficiency involving vision, hearing and the vestibular system. The purpose of this study is to report on the functional data (i.e. electroretinography, visual fields, visual acuity) of patients with retinitis pigmentosa (RP) due to Usher syndrome that were collected in a multicentre European study (TREATRUSH). Methods: A total of 268 genetically confirmed USH patients underwent electrophysiological examinations in the context of multimodal ophthalmological examination in the study (75 USH1, 189 USH2 and four USH3). Full-field electroretinography (ERG) was performed according to ISCEV standards, visual field determination was carried out with either the Octopus or Goldmann perimeters and visual acuity was examined with either ETDRS or Snellen charts. The data were compared between USH subtypes (USH1/USH2/USH3) and correlated with age. Results: Visual acuity decreases significantly with age for both USH1 and USH2 (p < 0.001), without a difference between the two cohorts. When corrected for age, the preserved kinetic visual field was significantly larger in USH2 than in USH1 (p = 0.04). Furthermore, the preserved kinetic visual field area showed a significant decrease with age (based on an exponential fit) in both USH1 and USH2 (p < 0.001). In USH1 patients, however, the visual field was already vastly reduced at an early age. The ERG results were abnormal in all patients. Detectable data for scotopic ERG were obtained from nine patients, and data of photopic ERG were obtained from 24 patients, without a difference between USH1 and USH2 subtypes. Conclusions: There are differences in the phenotypes of RP in USH subtypes, most visible in the progression of visual fields between USH1 and USH2. The perimetric reduction occurs earlier in USH1 than in USH2. In both subtypes, visual acuity decreases significantly with age and the ERG is not detectable already at early ages.
- Published
- 2019
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13. Usher Syndrome and Color Vision
- Author
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Ieva Sliesoraityte, Susanne Kohl, Stephanie Hipp, Francesca Simonelli, Ditta Zobor, Saddek Mohand-Said, José-Alain Sahel, Isabelle Audo, Anne Kurtenbach, Christoph Kernstock, Marko Hawlina, Crystel Bonnet, Francesco Testa, Ana Fakin, Katarina Stingl, Christine Petit, Eberhart Zrenner, Gesa Hahn, Institute for Ophthalmic Research [Tübingen, Germany] (Centre for Ophthalmology), University of Tübingen, Center for Ophthalmology, Institute for Ophthalmic research Tuebingen, Institut de la Vision, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Ecole Doctorale Complexité du Vivant (ED515), Sorbonne Université (SU), Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts (CHNO), Institut Arthur Vernes, University Medical Centre Ljubljana [Ljubljana, Slovenia] (UMCL), Università degli studi della Campania 'Luigi Vanvitelli', Génétique et Physiologie de l'Audition, Institut Pasteur [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU), Chaire Génétique et physiologie cellulaire, Collège de France (CdF (institution)), Università degli studi della Campania 'Luigi Vanvitelli' = University of the Study of Campania Luigi Vanvitelli, Institut Pasteur [Paris] (IP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU), Collège de France - Chaire Génétique et physiologie cellulaire, Kurtenbach, Anne, Hahn, Gesa, Kernstock, Christoph, Hipp, Stephanie, Zobor, Ditta, Stingl, Katarina, Kohl, Susanne, Bonnet, Crystel, Mohand-Saïd, Saddek, Sliesoraityte, Ieva, Sahel, José-Alain, Audo, Isabelle, Fakin, Ana, Hawlina, Marko, Testa, Francesco, Simonelli, Francesca, Petit, Christine, and Zrenner, Eberhart
- Subjects
0301 basic medicine ,Male ,Visual acuity ,genetic structures ,Usher syndrome ,[SDV]Life Sciences [q-bio] ,MESH: Color Perception Tests ,Visual Acuity ,Color Vision Defects ,030105 genetics & heredity ,MESH: Visual Acuity ,0302 clinical medicine ,Confusion ,MESH: Genetic Association Studies ,MESH: Aged ,MESH: Middle Aged ,Color Perception Tests ,medicine.diagnostic_test ,Middle Aged ,Sensory Systems ,MESH: Young Adult ,Female ,medicine.symptom ,Usher Syndromes ,Adult ,medicine.medical_specialty ,Adolescent ,Color vision ,03 medical and health sciences ,Cellular and Molecular Neuroscience ,Young Adult ,Ophthalmology ,medicine ,otorhinolaryngologic diseases ,Humans ,Color perception test ,retinal dystrophy ,MESH: Usher Syndromes ,Genetic Association Studies ,Hue ,Aged ,MESH: Adolescent ,MESH: Color Vision Defects ,MESH: Humans ,business.industry ,MESH: Adult ,medicine.disease ,eye diseases ,MESH: Male ,color vision ,Color loss ,030221 ophthalmology & optometry ,business ,MESH: Female - Abstract
Purpose: The aim of this study is to report on the results of color vision testing in a European cohort of patients with Usher syndrome (USH). We describe the results in relation to Usher type (USH1 and USH2), age and visual acuity. Methods and methods: The color vision of 220 genetically confirmed adult USH patients, aged 18–70 years, was analyzed with one of three methods: the Farnsworth D-15 Dichotomous test (D-15) along with the Lanthony desaturated 15 Hue tests (D-15d), the Roth 28-Hue test, or the Ishihara 14-plate test. Visual acuity was measured with either the ETDRS or the SNELLEN charts. The Confusion index, the Selectivity index and the Confusion angle were calculated for the panel tests and used for analysis. The numbers of plates that could not be read were analyzed for the Ishihara test. Results: For the panel tests, the degree of color loss (Confusion index) is similar in both subtypes of USH, but the polarization of error scores (Selectivity index) is significantly lower in USH1 than USH2, showing more diffuse errors than those found in USH2. There is no significant correlation between logMAR visual acuity and the Confusion or the Selectivity indices. Additionally, we find a significant correlation between patient age and the degree and the polarity of the loss only in USH2. There was no difference between USH1 and USH2 in the results of the Ishihara test. Conclusions: The examination of color vision in patients with USH shows a significant difference in the pattern of color vision loss in USH1 and USH2 patients, but not in the severity of the loss. In USH2, we find a correlation between patient age and the degree and the polarity of the loss. These results may be due to differences in the pathogenesis of retinal dystrophy in USH1 and USH2. Purpose: The aim of this study is to report on the results of color vision testing in a European cohort of patients with Usher syndrome (USH). We describe the results in relation to Usher type (USH1 and USH2), age and visual acuity.Methods and methods: The color vision of 220 genetically confirmed adult USH patients, aged 18-70years, was analyzed with one of three methods: the Farnsworth D-15 Dichotomous test (D-15) along with the Lanthony desaturated 15 Hue tests (D-15d), the Roth 28-Hue test, or the Ishihara 14-plate test. Visual acuity was measured with either the ETDRS or the SNELLEN charts. The Confusion index, the Selectivity index and the Confusion angle were calculated for the panel tests and used for analysis. The numbers of plates that could not be read were analyzed for the Ishihara test.Results: For the panel tests, the degree of color loss (Confusion index) is similar in both subtypes of USH, but the polarization of error scores (Selectivity index) is significantly lower in USH1 than USH2, showing more diffuse errors than those found in USH2. There is no significant correlation between logMAR visual acuity and the Confusion or the Selectivity indices. Additionally, we find a significant correlation between patient age and the degree and the polarity of the loss only in USH2. There was no difference between USH1 and USH2 in the results of the Ishihara test.Conclusions: The examination of color vision in patients with USH shows a significant difference in the pattern of color vision loss in USH1 and USH2 patients, but not in the severity of the loss. In USH2, we find a correlation between patient age and the degree and the polarity of the loss. These results may be due to differences in the pathogenesis of retinal dystrophy in USH1 and USH2.
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- 2018
- Full Text
- View/download PDF
14. Phenotype Variations Caused by Mutations in the RP1L1 Gene in a Large Mainly German Cohort.
- Author
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Zobor D, Zobor G, Hipp S, Baumann B, Weisschuh N, Biskup S, Sliesoraityte I, Zrenner E, and Kohl S
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- Adolescent, Adult, Aged, Child, Cohort Studies, Electroretinography, Female, Fluorescein Angiography, Germany, Humans, Macular Degeneration diagnostic imaging, Macular Degeneration physiopathology, Male, Middle Aged, Pedigree, Phenotype, Retina physiopathology, Retinitis Pigmentosa diagnostic imaging, Retinitis Pigmentosa physiopathology, Tomography, Optical Coherence, Young Adult, Eye Proteins genetics, Genetic Variation, Macular Degeneration genetics, Mutation, Retinitis Pigmentosa genetics
- Abstract
Purpose: Mutations in the retinitis pigmentosa-1-like-1 (RP1L1) gene are the major cause of autosomal dominant occult macular dystrophy (OCMD), while recessive mutations have been linked to autosomal recessive retinitis pigmentosa (arRP). We present the clinical phenotype of a large German OCMD cohort, as well as four RP patients., Methods: A total of 42 OCMD patients (27 families) and 4 arRP patients (3 families) with genetically confirmed mutations in RP1L1 were included. Genomic DNA was analyzed by targeted analysis of the c.133C>T;p.R45W mutation for all RP or macular dystrophy-related genes. All patients underwent ophthalmologic examination including psychophysical tests, electrophysiology, fundus autofluorescence (FAF), and spectral domain optical coherence tomography (SD-OCT). Follow-up time was up to 12 years., Results: In 25 OCMD index patients genomic testing revealed the heterozygous mutation c.133C>T;p.R45W in RP1L1; one patient was homozygous for the mutation. Two OCMD patients displayed the variants c.3599G>A;p.G1200D and c.2849G>A;p.R950H, respectively, in a heterozygous state. All OCMD patients showed characteristic clinical findings and typical microstructural photoreceptor changes. Two arRP patients displayed the novel homozygous mutations c.3022C>T;p.Q1008* and c.1107G>A;p.W369*, respectively, while two RP-siblings carried the two heterozygous mutations c.455G>A;p.R152Q and c.5959C>T;p.Q1987*, the first also being novel. All arRP cases were mild with disease onset ≈30 years and preserved ERG-responses., Conclusions: OCMD phenotype showed consistent clinical findings including classical microstructural changes on SD-OCT. An important hallmark of RP1L1-related OCMD is the dominant family history with reduced penetrance. Furthermore, novel mutations in association with arRP were identified, outlining the complexity of the protein.
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- 2018
- Full Text
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