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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Detalhes bibliográficos
Main Authors: Wang, Erli, Sun, Shuna, Qiao, Bin, Duan, Wenyuan, Huang, Guoying, An, Yu, Xu, Shuhua, Zheng, Yufang, Su, Zhixi, Gu, Xun, Jin, Li, Wang, Hongyan
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2013
Assuntos:
Research Article
Acesso em linha: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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