Related Articles
GATA5 loss-of-function mutation in familial dilated cardiomyopathy
A novel GATA4 loss-of-function mutation responsible for familial dilated cardiomyopathy
Prevalence and spectrum of LRRC10 mutations associated with idiopathic dilated cardiomyopathy
A novel TBX20 loss‑of‑function mutation contributes to adult‑onset dilated cardiomyopathy or congenital atrial septal defect
GATA6 loss-of-function mutations contribute to familial dilated cardiomyopathy