Genetic and Phenotypic Characteristics of Congenital Hypothyroidism in a Chinese Cohort

BACKGROUND: The molecular etiology and the genotype–phenotype correlation of congenital hypothyroidism (CH) remain unclear. METHODS: We performed genetic analysis in 42 newborns with CH using whole-exome sequencing. Patients were divided into a single-gene group and a multi-gene group according to t...

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Detalles Bibliográficos
Autores principales: Long, Wei, Guo, Fang, Yao, Ruen, Wang, Ying, Wang, Huaiyan, Yu, Bin, Xue, Peng
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/PMC8446595/
https://www.ncbi.nlm.nih.gov/pubmed/34539567
http://dx.doi.org/10.3389/fendo.2021.705773

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446595/
https://www.ncbi.nlm.nih.gov/pubmed/34539567
http://dx.doi.org/10.3389/fendo.2021.705773

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