Cerebellar ataxia, neuropathy, hearing loss, and intellectual disability due to AIFM1 mutation.
Neurol Genet
; 6(3): e420, 2020 Jun.
Article
in En
| MEDLINE
| ID: mdl-32337346
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Type of study:
Prognostic_studies
Language:
En
Journal:
Neurol Genet
Year:
2020
Document type:
Article
Affiliation country:
Bélgica