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Variable clinical manifestation of a novel missense mutation in the alpha-tropomyosin (TPM1) gene in familial hypertrophic cardiomyopathy

CardiomyopathyFamilial Hypertrophic CardiomyopathyGeneticsPathologyCongenital Heart AnomalyVariable Clinical ManifestationMedicineCardiologyCardiovascular GeneticsNovel Missense Mutation