Variant of TSHR is Not a Frequent Cause of Congenital Hypothyroidism in Chinese Han Patients.

Peng XueYuqi YangQi YunYue CuiBin Yu Wei Long

Published in: International journal of general medicine (2021)

The prevalence of TSHR variants was 11.2%. Variant p.F525S was the most prevalent variant with an allele frequency of 0.016. The prevalence of TSHR variants was different from other populations.

Keyphrases

end stage renal disease
risk factors
copy number
newly diagnosed
ejection fraction
chronic kidney disease
gene expression
dna methylation
patient reported outcomes
smoking cessation