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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Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: Mary Ann Liebert, Inc. 2012
Témata:
Molecular Mechanisms of Disease
On-line přístup: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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