Condition: Atrial Septal Defect with Atrioventricular Conduction Defects
rs72554028
in
NKX2-5
gene and
Atrial Septal Defect with Atrioventricular Conduction Defects
PMID 25319568
2014 NKX2-6 mutation predisposes to familial atrial fibrillation.
PMID 24880466
2014 Novel and highly lethal NKX2.5 missense mutation in a family with sudden death and ventricular arrhythmia.