Unequal allelic expression of wild-type and mutated β-myosin in familial hypertrophic cardiomyopathy
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Familial hypertrophic cardiomyopathy (FHC) is an autosomal dominant disease, which in about 30% of the patients is caused by missense mutations in one allele of the β-myosin heavy chain (β-MHC) gene (MYH7). To address potential molecular mechanisms underlyin... ...
