Alpers-Huttenlocher syndrome caused by a novel compound heterozygous mutation of POLG gene: a case report.
- Author:
Yan-Feng ZHANG
1
;
Jiang-Tao WANG
;
Jian-Bo GAO
;
Yan-Ying LYU
;
Jian-Min LIANG
;
Fei-Yong JIA
;
Yin-Bo CHEN
;
Yun-Peng HAO
Author Information
- Publication Type:Case Reports
- MeSH: DNA Polymerase gamma; DNA-Directed DNA Polymerase; genetics; Diffuse Cerebral Sclerosis of Schilder; diagnosis; drug therapy; etiology; genetics; Heterozygote; Humans; Infant; Male; Mutation
- From: Chinese Journal of Contemporary Pediatrics 2017;19(5):498-501
- CountryChina
- Language:Chinese
