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Phenotypic variability in a dystonia family with mutations in the manganese transporter gene
- Source :
- Movement Disorders, 28, 685-6, Movement Disorders, 28(5), 685-686. John Wiley & Sons Inc., Movement Disorders, 28, 5, pp. 685-6
- Publication Year :
- 2013
-
Abstract
- Item does not contain fulltext
- Subjects :
- Genetics
Dystonia
Mutation
business.industry
DCN MP - Plasticity and memory
Transporter gene
chemistry.chemical_element
DCN PAC - Perception action and control
Manganese
Glycostation disorders [IGMD 4]
medicine.disease
medicine.disease_cause
Phenotype
Clinical neurology
Genomic disorders and inherited multi-system disorders [IGMD 3]
Human Movement & Fatigue [DCN MP - Plasticity and memory NCEBP 10]
Neurology
chemistry
medicine
Neurology (clinical)
Glycostation disorders [DCN PAC - Perception action and control IGMD 4]
business
DCN NN - Brain networks and neuronal communication
Neuroscience
Dystonic disorder
Subjects
Details
- ISSN :
- 08853185
- Database :
- OpenAIRE
- Journal :
- Movement Disorders, 28, 685-6, Movement Disorders, 28(5), 685-686. John Wiley & Sons Inc., Movement Disorders, 28, 5, pp. 685-6
- Accession number :
- edsair.doi.dedup.....d0fcc3690050e0b56426c54d6be86df0