Mutation screening of the TPO gene in a cohort of 192 Chinese patients with congenital hypothyroidism

OBJECTIVES: Defects in the human thyroid peroxidase (TPO) gene are reported to be one of the causes of congenital hypothyroidism (CH) due to dyshormonogenesis. The aim of this study was to examine the TPO mutation spectrum and prevalence among patients with CH in the Guangxi Zhuang Autonomous Region...

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Detalhes bibliográficos
Publicado no:BMJ Open
Main Authors: Fu, Chunyun, Xie, Bobo, Zhang, Shujie, Wang, Jin, Luo, Shiyu, Zheng, Haiyang, Su, Jiasun, Hu, Xuyun, Chen, Rongyu, Fan, Xin, Luo, Jingsi, Gu, Xuefan, Chen, Shaoke
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Publishing Group 2016
Assuntos:
Diabetes and Endocrinology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4874165/
https://ncbi.nlm.nih.gov/pubmed/27173810
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bmjopen-2015-010719
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