Investigation of the relationship between G395R mutation of human sodium/iodide symporter and congenital hypothyroidism
- VernacularTitle:人钠/碘转运体基因G395R与先天性甲状腺功能减退症相关
- Author:
Shengli YAN
;
Zhen ZHAO
;
Ping FU
- Publication Type:Journal Article
- Keywords:
Hypothyroidism, congenital;
Gene mutation;
Sodium/iodide symporter
- From:
Chinese Journal of Endocrinology and Metabolism
1985;0(02):-
- CountryChina
- Language:Chinese
-
Abstract:
The G395R mutation of human sodium/iodide symporter gene was investigated by PCR-RFLP in 52 children with congenital hypothyroidism and 106 health children. The result suggested that G395R mutation may not be the main cause of congenital hypothyroidism in Qingdao.
