PITX2c Loss-of-Function Mutations Responsible for Congenital Atrial Septal Defects

Congenital heart disease (CHD) is the most common form of developmental anomaly and is the leading non-infectious cause of infant mortality. A growing body of evidence demonstrates that genetic risk factors are involved in the pathogenesis of CHD. However, CHD is a genetically heterogeneous disease...

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Detalhes bibliográficos
Main Authors: Yuan, Fang, Zhao, Lan, Wang, Juan, Zhang, Wei, Li, Xin, Qiu, Xing-Biao, Li, Ruo-Gu, Xu, Ying-Jia, Xu, Lei, Qu, Xing-Kai, Fang, Wei-Yi, Yang, Yi-Qing
Formato: Artigo
Idioma:Inglês
Publicado em: Ivyspring International Publisher 2013
Assuntos:
Research Paper
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3753420/
https://ncbi.nlm.nih.gov/pubmed/23983605
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7150/ijms.6809
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