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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2018
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Materias: | |
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 |
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