Clinical profile in arrhythmogenic cardiomyopathy and a recessive plakophilin-2 gene mutation
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DOI: 10.1016/j.ihj.2017.10.010
Abstract: Objective Arrhythmogenic cardiomyopathy (ACM) is not an uncommon cause of cardiac morbidity in Kashmir valley. This study was designed to document various clinical features and to sequence exons 11 and 12 of plakophilin 2 (PKP2)… read more here.
Keywords: mutation; acm patients; recessive plakophilin; arrhythmogenic cardiomyopathy ... See more keywords