Related Articles
Somatic GATA5 mutations in sporadic tetralogy of Fallot
GATA5 loss-of-function mutation in familial dilated cardiomyopathy
NR2F2 loss‑of‑function mutation is responsible for congenital bicuspid aortic valve
A novel GATA5 loss-of-function mutation underlies lone atrial fibrillation
A novel <em>KLF13</em> mutation underlying congenital patent ductus arteriosus and ventricular septal defect, as well as bicuspid aortic valve