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