Familial Hypertrophic Cardiomyopathy Associated with Cardiac β-Myosin Heavy Chain and Troponin I Mutations
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[1] Christine E Seidman,et al. A Contemporary Approach to Hypertrophic Cardiomyopathy , 2006, Circulation.
[2] P. Elliott,et al. Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy. , 2004, Journal of the American College of Cardiology.
[3] A. Gomes,et al. Cellular and molecular aspects of familial hypertrophic cardiomyopathy caused by mutations in the cardiac troponin I gene , 2004, Molecular and Cellular Biochemistry.
[4] A. Tajik,et al. Prevalence and age-dependence of malignant mutations in the beta-myosin heavy chain and troponin T genes in hypertrophic cardiomyopathy: a comprehensive outpatient perspective. , 2002, Journal of the American College of Cardiology.
[5] A. Marian. Modifier genes for hypertrophic cardiomyopathy. , 2002, Current opinion in cardiology.
[6] J. Seidman,et al. Sarcomere Protein Gene Mutations in Hypertrophic Cardiomyopathy of the Elderly , 2002, Circulation.
[7] D. Fatkin,et al. Molecular mechanisms of inherited cardiomyopathies. , 2002, Physiological reviews.
[8] J. Seidman,et al. A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy. , 2001, Journal of molecular and cellular cardiology.
[9] J. Seidman,et al. Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy. , 1992, The New England journal of medicine.
[10] Anne M Murphy,et al. Heart failure, myocardial stunning, and troponin: a key regulator of the cardiac myofilament. , 2006, Congestive heart failure.