Related Articles

• A novel TBX5 loss-of-function mutation associated with sporadic dilated cardiomyopathy
• A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias
• A novel <em>KLF13</em> mutation underlying congenital patent ductus arteriosus and ventricular septal defect, as well as bicuspid aortic valve
• GATA6 loss-of-function mutations contribute to familial dilated cardiomyopathy
• GATA5 loss-of-function mutation in familial dilated cardiomyopathy