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

Publisher： Spandidos Publications

E-ISSN： 1791-244X|35|2|478-486

ISSN： 1107-3756

Source： International Journal of Molecular Medicine, Vol.35, Iss.2, 2015-01, pp. : 478-486

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Abstract

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