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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Oncotarget
Autors principals: Liu, Shiguo, Wang, Xueqin, Zou, Hui, Ge, Yinlin, Wang, Fang, Wang, Yangang, Yan, Shengli, Xia, Hongfei, Xing, Mingzhao
Format: Artigo
Idioma:Inglês
Publicat: Impact Journals LLC 2017
Matèries:
Research Paper
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5352434/
https://ncbi.nlm.nih.gov/pubmed/28060725
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.14419
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars