Late-onset Leigh syndrome with m.9176T>C mutation in the mitochondrial ATPase 6 gene.
Pediatr Int
; 61(10): 1055-1056, 2019 Oct.
Article
in En
| MEDLINE
| ID: mdl-31625254
Full text:
1
Database:
MEDLINE
Main subject:
Leigh Disease
/
Mitochondrial Proton-Translocating ATPases
/
Mutation
Limits:
Child
/
Humans
/
Male
Language:
En
Journal:
Pediatr Int
Journal subject:
PEDIATRIA
Year:
2019
Type:
Article
Affiliation country:
Japan