Novel GATA6 Mutations Associated with Congenital Ventricular Septal Defect or Tetralogy of Fallot

Congenital heart disease (CHD) is the most common form of developmental malformation and is the leading noninfectious cause of infant mortality. Emerging evidence indicates that genetic defects are involved in the pathogenesis of CHD. Nevertheless, CHD is genetically heterogeneous, and the molecular...

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Detalhes bibliográficos
Main Authors: Wang, Juan, Luo, Xue-Jiao, Xin, Yuan-Feng, Liu, Yi, Liu, Zhong-Min, Wang, Qian, Li, Ruo-Gu, Fang, Wei-Yi, Wang, Xiao-Zhou, Yang, Yi-Qing
Formato: Artigo
Idioma:Inglês
Publicado em: Mary Ann Liebert, Inc. 2012
Assuntos:
Molecular Mechanisms of Disease
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3482375/
https://ncbi.nlm.nih.gov/pubmed/23020118
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/dna.2012.1814
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