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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2016
Materias:
Diabetes and Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4874165/
https://www.ncbi.nlm.nih.gov/pubmed/27173810
http://dx.doi.org/10.1136/bmjopen-2015-010719

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4874165/
https://www.ncbi.nlm.nih.gov/pubmed/27173810
http://dx.doi.org/10.1136/bmjopen-2015-010719

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