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Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy

Sara L. Van Driest, BA^*, Michele A. Jaeger, BA^*, Steve R. Ommen, MD, FACC, Melissa L. Will, BS^*, Bernard J. Gersh, MD, FACC, A. Jamil Tajik, MD, FACC and Michael J. Ackerman, MD, PhD, FACC^*,*

^* Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine, Rochester, Minnesota, USA
Department of Internal Medicine/Division of Cardiovascular Diseases, Mayo Clinic College of Medicine, Rochester, Minnesota, USA
Department of Pediatric and Adolescent Medicine/Division of Pediatric Cardiology, Mayo Clinic College of Medicine, Rochester, Minnesota, USA

View larger version (34K): [in a new window]   Figure 1 Distribution of mutations in the MYH7 gene. In the schematic diagram, vertical lines symbolize the exons of the gene and unfilled vertical lines represent untranslated regions. Mutations identified in this cohort are identified above the exons. * = a novel, not previously published mutation. For mutations found in more than one individual in the cohort, the mutation frequency is indicated in parentheses. All previously reported exonic mutations not found in this cohort are identified below the exons (11).