6Freiburg A,Gautel M. A molecular map of the interactions between titin and myosin-binding protein C: implications for sarcomeric assembly in familial hypertrophic cardiomyopathy[J].Eur J Biochem,1996,235 : 317.
7Van Driest SI., Vasile VC, Ommen SR, et al. Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy [J].J Am Coll Cardiol, 2004, 44 :1903.
8Gomes AV,Barnes JA,Harada K,et aI. Role of troponin T in disease[J]. Mol Cell Biochem, 2004,263 :115.
9Sweeney HL, Teng HS,Yang Z,et al. Functional analyses of troponin T mutations that cause hypertrophic cardiomyopathy:insights into disease pathogenesis and troponin function[J].J Lipid Res,1999,40: 178.
10Anan R,Shono H,Kisanuki A,et al. Patients with familial hypertrophic cardiomyopathy caused by a Phe110lle missense mutation in the cardiac troponin T gene have variahte cardiac morphologies and a favorable prognosis[J]. Circulation, 1998.98 : 391.
3Marian AJ, Roberts R. The molecular genetic basis for hypertrophic cardiomyopathy. J Mol Cell Cardiol, 2001, 33:655-670.
4Seidman JG, Seidman C. The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms. Cell, 2001, 104:557-567.
5Bonne G, Carrier L, Richard P, et al. Familial hypertrophic cardiomyopathy: from mutations to functional defects. Circ Res, 1998, 83:580-593.
6Rayment I, Rypniewski RW, Schmidt-Base K, et al. Three-dimensional structure of myosin subfragment-1: a molecular motor. Science, 1993, 261:50-58.
7Anan R, Greve G, Thierfelder L, et al. Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy. J Clin Invest, 1994, 93:280-285.
8Niimura H, Bachinski LL, Sangwatanaro JS, et al. Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy. N Engl J Med, 1998, 338:1248-1257.
9Ortlepp JR, Vosberg HP, Reith S, et al. Genetic polymorphisms in the renin- angiotensin -aldosterone system associated with expression of left ventricular hypertrophy in hypertrophic cardiomyopathy: a study of five polymorphic genes in a family with a disease causing mutation in the myosin binding protein C gene. Heart, 2002, 87:270-275.
10Futterman LG, Myerburg R. Sudden death in athletes: an update. Sports Med, 1998, 26:335-350.
