1Anan R,Shono H,Kisanuki A,et al.Patients with familial hypertrophic cardiomyopathy caused by a Phe110Ile missense mutation in the cardiac troponin T gene have variable cardiac morphologies and a favorable prognosis[J].Circula-tion,1998,98(5):391-397.
2Miliou AL,Anastasakis AL,D′Cruz LG,et al.Low prevalence of cardiac troponin T mutations in a Greek hypertrophic cardiomyopathy cohort[J].Heart,2005,91(7):966-967.
3Charron P,Dubourg O,Desnos M,et al.Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene[J].Circulation,1998,97(22):2230-2236.
4Elliott PM,Poloniecki J,Dickie S,et al.Sudden death in hypertrophic cardiomyopathy:Identification of high risk patients[J].JACC,2000,36(7):2212-2218.
8Maki S,Ikeda H,Muro A,et al.Predictors of sudden cardiac death in hypertrophic cardiomyopathy[J].Am J Cardiol,1998,82(6):774-778.
9Elliott PM,Gimeno Blanes JR,Mahon NG,et al.Relation between severity of left-ventricular hypertrophy and prognosis in patients with hypertrophic cardiomyopathy[J].Lancet,2001,357:420-424.
10Maron BJ.Contemporary considerations for risk stratification,sudden death and prevention in hypertrophic cardiomyopathy[J].Heart,2003,89(9):977-978.