Identification of Functional Mutations in GATA4 in Patients with Congenital Heart Disease

Congenital heart disease (CHD) is one of the most prevalent developmental anomalies and the leading cause of noninfectious morbidity and mortality in newborns. Despite its prevalence and clinical significance, the etiology of CHD remains largely unknown. GATA4 is a highly conserved transcription fac...

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Autors principals: Wang, Erli, Sun, Shuna, Qiao, Bin, Duan, Wenyuan, Huang, Guoying, An, Yu, Xu, Shuhua, Zheng, Yufang, Su, Zhixi, Gu, Xun, Jin, Li, Wang, Hongyan
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2013
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3633926/
https://ncbi.nlm.nih.gov/pubmed/23626780
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0062138
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