Condition: VENTRICULAR SEPTAL DEFECT 3
rs375086983
in
NKX2-5
gene and
VENTRICULAR SEPTAL DEFECT 3
PMID 21165553
2011 A novel NKX2-5 mutation in familial ventricular septal defect.
PMID 21110066
2010 Mutations of the GATA4 and NKX2.5 genes in Chinese pediatric patients with non-familial congenital heart disease.