Identification and characterization of novel PAX8 mutations in Congenital Hypothyroidism(CH) in a Chinese population

OBJECTIVE: Based on mutations in PAX8 is associated with thyroid dysgenesis. We aim to identify and characterize PAX8 mutations in a large cohort of congenital hypothyroidism(CH) from thyroid dysgenesis in Chinese population. METHODS: We screened 453 unrelated Chinese patients with CH from thyroid d...

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Detalles Bibliográficos
Autores principales: Liu, Shiguo, Wang, Xueqin, Zou, Hui, Ge, Yinlin, Wang, Fang, Wang, Yangang, Yan, Shengli, Xia, Hongfei, Xing, Mingzhao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352434/
https://www.ncbi.nlm.nih.gov/pubmed/28060725
http://dx.doi.org/10.18632/oncotarget.14419

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352434/
https://www.ncbi.nlm.nih.gov/pubmed/28060725
http://dx.doi.org/10.18632/oncotarget.14419

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