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Identification of three novel pathogenic mutations in sarcomere genes associated with familial hypertrophic cardiomyopathy based on multi-omics study

CardiomyopathyMendelian DisorderFamilial Hypertrophic CardiomyopathyGenetic DisorderMedicineGeneticsMulti-omics StudyPathologyOmicsSarcomere GenesDisease Gene IdentificationMolecular DiagnosticsCardiovascular Genetics