KCNJ11 gene mutation in 3 cases with neonatal diabetes mellitus / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 682-683, 2010.
Article
de Zh
| WPRIM
| ID: wpr-387948
Bibliothèque responsable:
WPRO
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.
Texte intégral:
1
Indice:
WPRIM
langue:
Zh
Texte intégral:
Chinese Journal of Endocrinology and Metabolism
Année:
2010
Type:
Article