A case of malonyl-CoA decarboxylase deficiency: clinical and genetic study.
- Author:
Jing PENG
1
;
Ling-Qian WU
;
Ming-Xing ZHOU
;
Le ZHONG
;
Fei YIN
Author Information
1. Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China.
- Publication Type:Case Reports
- MeSH:
Carboxy-Lyases;
deficiency;
genetics;
Child, Preschool;
Humans;
Male;
Polymorphism, Single Nucleotide
- From:
Chinese Journal of Contemporary Pediatrics
2012;14(11):879-880
- CountryChina
- Language:Chinese
