The genetic characteristics of congenital hypothyroidism in China by comprehensive screening of 21 candidate genes

OBJECTIVE: Congenital hypothyroidism (CH), the most common neonatal metabolic disorder, is characterized by impaired neurodevelopment. Although several candidate genes have been associated with CH, comprehensive screening of causative genes has been limited. DESIGN AND METHODS: One hundred ten patie...

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Detalhes bibliográficos
Publicado no:Eur J Endocrinol
Main Authors: Sun, Feng, Zhang, Jun-Xiu, Yang, Chang-Yi, Gao, Guan-Qi, Zhu, Wen-Bin, Han, Bing, Zhang, Le-Le, Wan, Yue-Yue, Ye, Xiao-Ping, Ma, Yu-Ru, Zhang, Man-Man, Yang, Liu, Zhang, Qian-Yue, Liu, Wei, Guo, Cui-Cui, Chen, Gang, Zhao, Shuang-Xia, Song, Ke-Yi, Song, Huai-Dong
Formato: Artigo
Idioma:Inglês
Publicado em: Bioscientifica Ltd 2018
Assuntos:
Clinical Study
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5958289/
https://ncbi.nlm.nih.gov/pubmed/29650690
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EJE-17-1017
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