Clinical and mutational spectrum of Japanese patients with Charcot-Marie-Tooth disease caused by GDAP1 variants.
Clin Genet
; 92(3): 274-280, 2017 Sep.
Article
in En
| MEDLINE
| ID: mdl-28244113
Key words
Full text:
1
Database:
MEDLINE
Main subject:
Phenotype
/
Charcot-Marie-Tooth Disease
/
Mutation
/
Nerve Tissue Proteins
Type of study:
Prognostic_studies
Limits:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Female
/
Humans
/
Male
/
Middle aged
Country/Region as subject:
Asia
Language:
En
Year:
2017
Type:
Article