Apical hypertrophic cardiomyopathy due to a de novo mutation Arg719Trp of the b-myosin heavy chain gene and cardiac arrest in childhood A case report and family study: A case report and family study

SummaryHypertrophic cardiomyopathy (HCM) is a myocardial disease with variable phenotpye and genotype. To demonstrate that the mutation Arg719Trp in the cardiac β-myosin heavy chain (βMHC) gene is a high risk factor for sudden death and can be associated with an unusual apical non-obstructive HCM, w...

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