Mitochondrial ATP synthase deficiency due to 8993T > G mutation on ATP6 gene.
- Author:
Yan-yan MA
;
Tong-fei WU
;
Yu-peng LIU
- Publication Type:Case Reports
- MeSH: Female; Humans; Infant; Mitochondrial Proton-Translocating ATPases; deficiency; genetics; Mutation
- From: Chinese Journal of Pediatrics 2011;49(7):557-558
- CountryChina
- Language:Chinese