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Published in 2022 at "Circulation"
DOI: 10.1161/circulationaha.120.049261
Abstract: Background: Arrhythmogenic cardiomyopathy (ACM) is an inherited genetic disorder of desmosomal dysfunction, and PKP2 (plakophilin-2) has been reported to be the most common disease-causing gene when mutation-positive. In the early concealed phase, the ACM heart…
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Keywords:
pkp2 het;
pkp2;
actin expression;
contraction ... See more keywords