KCNJ11 gene mutation in 3 cases with neonatal diabetes mellitus
10.3760/cma.j.issn.1000-6699.2010.08.014
- VernacularTitle:三例新生儿糖尿病KCNJ11基因突变分析
- Author:
Yanmei SANG
;
Guichen NI
;
Yi GU
;
Min LIU
- Publication Type:Journal Article
- Keywords:
Neonatal diabetes mellitus;
KCNJ 11 gene;
ATP-sensitive K channel
- From:
Chinese Journal of Endocrinology and Metabolism
2010;26(8):682-683
- CountryChina
- Language:Chinese
-
Abstract:
KCNJ11 gene mutation was searched in 3 families with neonatal diabetes. A KCNJ11 175 G>A (V59M) mutation was found in one child, while no KCNJ11 gene mutation was found in his parents. No mutation was found in the other two families. The result indicated that KCNJ11 gene mutation might lead to the onset of neonatal diabetes mellitus in Chinese.