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Reply: The expanding neurological phenotype of DNM1L-related disorders
- Source :
- Brain-A Journal of Neurology, Brain-A Journal of Neurology, Oxford University Press (OUP), 2018, 141 (4), pp.e29-e29. ⟨10.1093/brain/awy027⟩, Brain-A Journal of Neurology, 2018, 141 (4), pp.e29-e29. ⟨10.1093/brain/awy027⟩
- Publication Year :
- 2018
- Publisher :
- HAL CCSD, 2018.
-
Abstract
- Comment on :Mutations in DNM1L, as in OPA1, result in dominant optic atrophy despite opposite effects on mitochondrial fusion and fission. [Brain. 2017]The expanding neurological phenotype of DNM1L-related disorders. [Brain. 2018]; International audience; Letter to the editor
- Subjects :
- 0301 basic medicine
Dynamins
[SDV]Life Sciences [q-bio]
education
Bioinformatics
Mitochondrial Dynamics
GTP Phosphohydrolases
Mitochondrial Proteins
03 medical and health sciences
0302 clinical medicine
Text mining
Optic Atrophy, Autosomal Dominant
Medicine
Humans
ComputingMilieux_MISCELLANEOUS
business.industry
Phenotype
eye diseases
[SDV] Life Sciences [q-bio]
030104 developmental biology
Mutation
Neurology (clinical)
business
Microtubule-Associated Proteins
030217 neurology & neurosurgery
Subjects
Details
- Language :
- English
- ISSN :
- 00068950 and 14602156
- Database :
- OpenAIRE
- Journal :
- Brain-A Journal of Neurology, Brain-A Journal of Neurology, Oxford University Press (OUP), 2018, 141 (4), pp.e29-e29. ⟨10.1093/brain/awy027⟩, Brain-A Journal of Neurology, 2018, 141 (4), pp.e29-e29. ⟨10.1093/brain/awy027⟩
- Accession number :
- edsair.doi.dedup.....0b630bc85e89b94a2cc2225e06352c8e
- Full Text :
- https://doi.org/10.1093/brain/awy027⟩