Screening of HHEX Mutations in Chinese Children with Thyroid Dysgenesis

OBJECTIVE: Congenital hypothyroidism (CH) is a frequent neonatal endocrine disease with an incidence of about 1:2500 worldwide. Although thyroid dysgenesis (TD) is the most frequent cause of CH cases, its pathogenesis remains unclear. The aim of this study was to screen the hematopoietically-express...

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Detalles Bibliográficos
Autores principales: Liu, Shiguo, Chai, Jian, Zheng, Guohua, Li, Huichao, Lu, Deguo, Ge, Yinlin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4805044/
https://www.ncbi.nlm.nih.gov/pubmed/26757609
http://dx.doi.org/10.4274/jcrpe.2456

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4805044/
https://www.ncbi.nlm.nih.gov/pubmed/26757609
http://dx.doi.org/10.4274/jcrpe.2456

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