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pubmed-article:8791411pubmed:abstractTextMutations in several muscle structural proteins (the myosin heavy chain, alpha tropomyosin, cardiac troponin T and myosin binding protein C) result in a genetically dominant heart disease, hypertrophic cardiomyopathy. Biochemical data from studies of mutant myosin suggest a dominant-negative mechanism for inheritance of this disease. The most likely primary defect is sarcomere dysfunction, which is followed by the major clinical symptoms.lld:pubmed
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pubmed-article:8791411pubmed:articleTitleContractile protein mutations and heart disease.lld:pubmed
pubmed-article:8791411pubmed:affiliationDepartment of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder 80309-0347, USA. vikstrom@stripe.colorado.edulld:pubmed
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