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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...
Autores principales: | Liu, Shiguo, Wang, Xueqin, Zou, Hui, Ge, Yinlin, Wang, Fang, Wang, Yangang, Yan, Shengli, Xia, Hongfei, Xing, Mingzhao |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
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 |
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