Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy.
Parkinsonism Relat Disord
; 63: 66-72, 2019 06.
Article
in En
| MEDLINE
| ID: mdl-30850329
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Cell Adhesion Molecules
/
Cerebellar Ataxia
/
Demyelinating Diseases
/
Neurodevelopmental Disorders
/
Nerve Growth Factors
Type of study:
Etiology_studies
/
Prognostic_studies
Limits:
Adolescent
/
Adult
/
Female
/
Humans
/
Male
Language:
En
Journal:
Parkinsonism Relat Disord
Journal subject:
NEUROLOGIA
Year:
2019
Document type:
Article
Affiliation country:
Italy
Country of publication:
United kingdom