Expanding the phenotype of IBA57 mutations: related leukodystrophy can remain asymptomatic.
J Hum Genet
; 63(12): 1223-1229, 2018 Dec.
Article
in En
| MEDLINE
| ID: mdl-30258207
Full text:
1
Database:
MEDLINE
Main subject:
Phenotype
/
Carrier Proteins
/
Hereditary Central Nervous System Demyelinating Diseases
/
Mutation
Limits:
Adult
/
Female
/
Humans
/
Male
Language:
En
Journal:
J Hum Genet
Journal subject:
GENETICA MEDICA
Year:
2018
Type:
Article
Affiliation country:
Japan