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

PURPOSE: To screen variants of the thyroid stimulating hormone receptor (TSHR) gene among congenital hypothyroidism (CH) patients. PATIENTS AND METHODS: We conducted a genetic screening of the TSHR gene in a cohort of 125 Chinese CH patients. Variants were detected by customized targeted next-genera...

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Detalles Bibliográficos
Autores principales: Xue, Peng, Yang, Yuqi, Yun, Qi, Cui, Yue, Yu, Bin, Long, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8349214/
https://www.ncbi.nlm.nih.gov/pubmed/34377013
http://dx.doi.org/10.2147/IJGM.S322726

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8349214/
https://www.ncbi.nlm.nih.gov/pubmed/34377013
http://dx.doi.org/10.2147/IJGM.S322726

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