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Academic Press

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Malignant Hypertrophic Cardiomyopathy Caused by the Arg723Gly Mutation in &bgr; -Myosin Heavy Chain Gene

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Homozygotes for a R869G Mutation in the &bgr; -myosin Heavy Chain Gene have a Severe Form of Familial Hypertrophic Cardiomyopathy

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Altered Regulation of Cardiac Muscle Contraction by Troponin T Mutations that Cause Familial Hypertrophic Cardiomyopathy

By Knollmann B.C.   Potter J.D.  

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Mutations in the cardiac troponin T gene show various prognoses in Japanese patients with hypertrophic cardiomyopathy

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Heart and Vessels, Vol. 28, Iss. 6, 2013-11 ,pp. : 785-794

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