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: Source Type: research