共 45 条
[1]
Maron B.J., Gardin J.M., Flack J.M., Et al., Prevalence of hypertrophic cardiomyopathy in a general population of young adults
[2]
echocardiographic analysis of 4111 subjects in the cardia study, Circulation, 92, pp. 785-789, (1995)
[3]
McKenna W.J., Deanfield J., Faruqui A., Et al., Prognosis in hypertrophic cardiomyopathy. Role of age and clinical, electrocardiographic and haemodynamic features, Am J Cardiol, 47, pp. 532-538, (1981)
[4]
Maron B.J., Wolfson J.K., Epstein S.E., Roberts W.C., Intramural ("small vessel") coronary artery disease in hypertrophic cardiomyopathy, J Am Coll Cardiol, 8, (1986)
[5]
Kimura A., Harada H., Park J.-E., Et al., Mutations in the cardiac troponin i gene associated with hypertrophic cardiomyopathy, Nat Genet, 16, pp. 379-382, (1997)
[6]
Jarcho J.A., McKenna W.J., Pare J.A., Et al., Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1, N Engl J Med, 321, pp. 1372-1378, (1989)
[7]
Thierfelder L., MacRae C., Watkins H., Et al., A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2, Proc Natl Acad Sci U S A, 90, pp. 6270-6274, (1993)
[8]
Watkins H., McRae C., Thierfelder L., Et al., A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3, Nat Genet, 3, pp. 333-337, (1993)
[9]
Bonne G., Carrier L., Bercovici J., Et al., Cardiac myosin binding protein c gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy, Nat Genet, 11, pp. 438-440, (1995)
[10]
Watkins H., Rozenzweig A., Hwang D.S., Et al., Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy, N Engl J Med, 326, pp. 1108-1114, (1992)