ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy
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DOI: 10.1007/s00380-017-1110-4
Abstract: Dilated cardiomyopathy (DCM) is a common primary myocardial disease leading to congestive heart failure, arrhythmia and sudden cardiac death. Increasing studies demonstrate substantial genetic determinants for DCM. Nevertheless, DCM is of substantial genetic heterogeneity, and… read more here.
Keywords: loss function; function mutation; dilated cardiomyopathy; zbtb17 ... See more keywords