Open AccessVariant of TSHR is Not a Frequent Cause of Congenital Hypothyroidism in Chinese Han Patients
Author(s) -
Peng Xue,
Yuqi Yang,
Yun Qi,
Yue Cui,
Bin Yu,
Wei Long
Publication year - 2021
Publication title -
international journal of general medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.722
H-Index - 36
ISSN - 1178-7074
DOI - 10.2147/ijgm.s322726
Subject(s) - medicine , allele , missense mutation , congenital hypothyroidism , cohort , allele frequency , thyrotropin receptor , gene , genetics , thyroid , graves' disease , mutation , biology