A Novel Missense Mutation of GATA4 in a Chinese Family with Congenital Heart Disease

BACKGROUND: Congenital heart disease (CHD) is the most prevalent type of birth defect in human, with high morbidity in infant. Several genes essential for heart development have been identified. GATA4 is a pivotal transcription factor that can regulate the cardiac development. Many GATA4 mutations h...

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Detalles Bibliográficos
Autores principales: Zhang, Xiaoqing, Wang, Jian, Wang, Bo, Chen, Sun, Fu, Qihua, Sun, Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4938561/
https://www.ncbi.nlm.nih.gov/pubmed/27391137
http://dx.doi.org/10.1371/journal.pone.0158904

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4938561/
https://www.ncbi.nlm.nih.gov/pubmed/27391137
http://dx.doi.org/10.1371/journal.pone.0158904

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