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A high risk phenotype of hypertrophic cardiomyopathy associated with a compound genotype of two mutated β-myosin heavy chain genes

Cardiac MuscleCardiomyopathyCompound GenotypeGeneticsGenetic EpidemiologyHigh Risk PhenotypePathologyHypertrophic CardiomyopathyMedicineCardiologyCardiovascular GeneticsCardiac Pathology