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International Journal of Molecular Medicine, Vol. 31, Iss. 5, 2013-05 ,pp. : 1119-1126

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A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias

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Novel GATA6 loss-of-function mutation responsible for familial atrial fibrillation

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A novel NKX2-5 mutation in familial ventricular septal defect

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A novel GATA5 loss-of-function mutation underlies lone atrial fibrillation

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