Familial Hypertrophic Cardiomyopathy Associated with a Novel Missense Mutation Affecting the ATP-binding Region of the Cardiac Beta-myosin Heavy Chain

By Bundgaard H.   Havndrup O.   Andersen P.S.   Larsen L.A.   Brandt N.J.   Vuust J.   Kjeldsen K.   Christiansen M.  

Journal of Molecular and Cellular Cardiology, Vol. 31, Iss. 4, 1999-04 ,pp. : 745-750

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Functional Consequences of the Mutations in Human Cardiac Troponin I Gene Found in Familial Hypertrophic Cardiomyopathy

By Takahashi-Yanaga F.   Morimoto S.   Harada K.   Minakami R.   Shiraishi F.   Ohta M.   Lu Q-W.   Sasaguri T.   Ohtsuki I.  

Journal of Molecular and Cellular Cardiology, Vol. 33, Iss. 12, 2001-12 ,pp. : 2095-2107

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

By Richard P.   Charron P.   Leclercq C.   Ledeuil C.   Carrier L.   Dubourg O.   desnos M.   Bouhour J-B.   Schwartz K.   Daubert J.C.   Komajda M.   Hainque B.  

Journal of Molecular and Cellular Cardiology, Vol. 32, Iss. 8, 2000-08 ,pp. : 1575-1583

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

By Enjuto M.   Francino A.   Navarro-López F.   Viles D.   Paré J-C.   Ballesta A.M.  

Journal of Molecular and Cellular Cardiology, Vol. 32, Iss. 12, 2000-12 ,pp. : 2307-2313

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Isometric Tension and Mutant Myosin Heavy Chain Content in Single Skeletal Myofibers from Hypertrophic Cardiomyopathy Patients

By Malinchik S.   Cuda G.   Podolsky R.J.   Horowits R.  

Journal of Molecular and Cellular Cardiology, Vol. 29, Iss. 2, 1997-02 ,pp. : 667-676

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