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    Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

    Hypertrophic cardiomyopathy (HCM), the most common cause of sudden death in the young, is an autosomal dominant disease characterized by ventricular hypertrophy accompanied by myofibrillar disarrays1. Linkage stu...

    Akinori Kimura, Haruhito Harada, Jeong-Euy Park, Hirofumi Nishi… in Nature Genetics (1997)