Prevalence and Spectrum of PITX2c Mutations Associated with Congenital Heart Disease

Congenital heart disease (CHD) is the most common form of birth defect and is the leading noninfectious cause of infant death. A growing body of evidence demonstrates that genetic risk factors are involved in the pathogenesis of CHD. However, CHD is a genetically heterogeneous disease and the geneti...

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Detalhes bibliográficos
Main Authors: Wang, Juan, Xin, Yuan-Feng, Xu, Wen-Jun, Liu, Zhong-Min, Qiu, Xing-Biao, Qu, Xin-Kai, Xu, Lei, Li, Xin, Yang, Yi-Qing
Formato: Artigo
Idioma:Inglês
Publicado em: Mary Ann Liebert, Inc. 2013
Assuntos:
Molecular Mechanisms of Disease
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3864367/
https://ncbi.nlm.nih.gov/pubmed/24083357
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/dna.2013.2185
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