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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3633926/
https://www.ncbi.nlm.nih.gov/pubmed/23626780
http://dx.doi.org/10.1371/journal.pone.0062138

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3633926/
https://www.ncbi.nlm.nih.gov/pubmed/23626780
http://dx.doi.org/10.1371/journal.pone.0062138

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