A patient with development delay and pallidal and cerebellar lesions caused by MBOAT7 gene variant.
- Author:
Shuang LI
1
;
Cui Jie WEI
1
;
Fen Fen XU
1
;
Ying ZHU
2
;
Xin Hua BAO
1
Author Information
- Publication Type:Journal Article
- MeSH: Humans; Genotype; Non-alcoholic Fatty Liver Disease; Acyltransferases/genetics*; Membrane Proteins/genetics*
- From: Chinese Journal of Pediatrics 2023;61(11):1046-1048
- CountryChina
- Language:Chinese
