Identifying the thyroglobulin mutations from patients with congenital hypothyroidism  

作　　者：涂平辉 TU Pinghui(Dept Endocrinol,Shanghai Ninth People's Hosp,Shanghai Jiaotong Univ Med Sch,Shanghai 200001)

机构地区：[1]Dept Endocrinol,Shanghai Ninth People's Hosp,Shanghai Jiaotong Univ Med Sch,Shanghai 200001

出　　处：《China Medical Abstracts(Internal Medicine)》2023年第4期214-214,共1页中国医学文摘（内科学分册（英文版）

摘　　要：Objective To identify mutations of the thyroglobulin(TG)gene and inheritance patterns in Chinese patients with congenital hypothyroidism.Methods Clinical data of 235 children with congenital hypothyroidism and some of their families were collected from 2014 to 2018,and peripheral blood samples were collected for DNA extraction.

关 键 词：HYPOTHYROIDISM CONGENITAL GLOBULIN 

分 类 号：R581.2[医药卫生—内分泌]