Analysis of Mutation Spectra of 28 Pathogenic Genes Associated With Congenital Hypothyroidism in the Chinese Han Population

PURPOSE: Congenital hypothyroidism (CH) is the most common neonatal endocrine disease; its early detection ensures successful treatment and prevents complications. However, its molecular etiology remains unclear. METHODS: We used second-generation sequencing to detect 28 pathogenic genes in 15 Chine...

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Detalles Bibliográficos
Autores principales: Huang, Miao, Lu, Xiyan, Dong, Guoqing, Li, Jianxu, Chen, Chengcong, Yu, Qiuxia, Li, Mingzhu, Su, Yueyue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8284857/
https://www.ncbi.nlm.nih.gov/pubmed/34276565
http://dx.doi.org/10.3389/fendo.2021.695426

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8284857/
https://www.ncbi.nlm.nih.gov/pubmed/34276565
http://dx.doi.org/10.3389/fendo.2021.695426

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