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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Mary Ann Liebert, Inc. 2012
Pynciau:
Molecular Mechanisms of Disease
Mynediad Ar-lein: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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