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Homozygotes for a R869G Mutation in the β -myosin Heavy Chain Gene have a Severe Form of Familial Hypertrophic Cardiomyopathy

Cardiac MuscleCardiomyopathyMendelian DisorderFamilial Hypertrophic CardiomyopathyGenetic DisorderGeneticsGenetic EpidemiologyPathologyMolecular GeneticsSevere FormMedicineR869g MutationCardiovascular Genetics