Mutations of NKX2.5 and GATA4 genes in the development of congenital heart disease
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference29 articles.
1. Germline mutations in NKX2-5, GATA4, and CRELD1 are rare in a Mexican sample of Down syndrome patients with endocardial cushion and septal heart defects;Alcantara-Ortigoza;Pediatr. Cardiol.,2015
2. beta-Myosin heavy chain variant Val606Met causes very mild hypertrophic cardiomyopathy in mice, but exacerbates HCM phenotypes in mice carrying other HCM mutations;Blankenburg;Circ. Res.,2014
3. Art27 interacts with GATA4, FOG2 and NKX2.5 and is a novel co-repressor of cardiac genes;Carter;PLoS One,2014
4. Problems of the neonates with congenital heart disease requiring early interventions: a regional report;Celik;Turk Pediatri Ars,2015
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