Hypertrophic Cardiomyopathy and Rare Genetic Mutations
Introduction: Hypertrophic cardiomyopathy (HCM) is a genetic disorder of cardiomyocytes, whose prevalence is approximately 1:500 in the general adult population, with a wide spectrum of clinical and morphological presentation.
Source: The Journal of Heart and Lung Transplantation - Category: Transplant Surgery Authors: , G. Campos, S. Mangini, S. Moraes, F. Bacal Source Type: research
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