A Chinese patient with glycogen storage disease type Ib caused by mutations in the glucose-6-phosphate translocase gene.
- Author:
Qian LIN
;
Bixia ZHENG
;
Mei LI
- Publication Type:Case Reports
- MeSH: Antiporters; genetics; Base Sequence; Female; Glycogen Storage Disease Type I; diagnosis; genetics; Humans; Infant; Monosaccharide Transport Proteins; genetics; Mutation; Polymerase Chain Reaction; Sequence Analysis, DNA
- From: Chinese Journal of Pediatrics 2014;52(1):58-60
- CountryChina
- Language:Chinese