Related Articles
TBX20 loss-of-function mutation contributes to double outlet right ventricle
HAND1 loss-of-function mutation contributes to congenital double outlet right ventricle
A novel HAND2 loss-of-function mutation responsible for tetralogy of Fallot
Novel PITX2c loss-of-function mutations associated with complex congenital heart disease
A novel TBX20 loss‑of‑function mutation contributes to adult‑onset dilated cardiomyopathy or congenital atrial septal defect