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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2018
Materias:
Clinical Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5958289/
https://www.ncbi.nlm.nih.gov/pubmed/29650690
http://dx.doi.org/10.1530/EJE-17-1017

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5958289/
https://www.ncbi.nlm.nih.gov/pubmed/29650690
http://dx.doi.org/10.1530/EJE-17-1017

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