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Volumn 62, Issue 12, 2009, Pages 1473-1477

Hypertrophic Cardiomyopathy. A Study of the Troponin-T Gene in 127 Spanish Families;Miocardiopatía hipertrófica. Estudio del gen de la troponina T en 127 familias españolas

Author keywords

Genetics; Hypertrophic cardiomyopathy; Sudden death; Troponin T

Indexed keywords

ARGININE; ASPARTIC ACID; LEUCINE; TROPONIN T;

EID: 75349113467     PISSN: 03008932     EISSN: 15792242     Source Type: Journal    
DOI: 10.1016/S0300-8932(09)73136-7     Document Type: Article
Times cited : (19)

References (13)
  • 1
    • 0029166817 scopus 로고
    • Recent advances in the molecular genetics of hypertrophic cardiomyopathy
    • Marian A.J., and Roberts R. Recent advances in the molecular genetics of hypertrophic cardiomyopathy. Circulation 92 (1995) 1336-1347
    • (1995) Circulation , vol.92 , pp. 1336-1347
    • Marian, A.J.1    Roberts, R.2
  • 2
    • 0025040392 scopus 로고
    • A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation
    • Geisterfer-Lowrance A.A., Kass S., Tanigawa G., Vosberg H.P., McKenna W., Seidman C.E., et al. A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation. Cell 62 (1990) 999-1006
    • (1990) Cell , vol.62 , pp. 999-1006
    • Geisterfer-Lowrance, A.A.1    Kass, S.2    Tanigawa, G.3    Vosberg, H.P.4    McKenna, W.5    Seidman, C.E.6
  • 3
    • 0037630018 scopus 로고    scopus 로고
    • Hypertrophic cardiomyopathy. Distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy
    • Richard P., Charron P., Carrier L., Ledeuil C., Cheav T., Pichereau C., et al. Hypertrophic cardiomyopathy. Distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy. Circulation 107 (2003) 2227-2232
    • (2003) Circulation , vol.107 , pp. 2227-2232
    • Richard, P.1    Charron, P.2    Carrier, L.3    Ledeuil, C.4    Cheav, T.5    Pichereau, C.6
  • 4
    • 0028902929 scopus 로고
    • Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy
    • Watkins H., McKenna W.J., Thierfelder L., Suk H.J., Anan R., O'Donoghue A., et al. Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy. N Engl J Med 332 (1995) 1058-1064
    • (1995) N Engl J Med , vol.332 , pp. 1058-1064
    • Watkins, H.1    McKenna, W.J.2    Thierfelder, L.3    Suk, H.J.4    Anan, R.5    O'Donoghue, A.6
  • 5
    • 0242572234 scopus 로고    scopus 로고
    • Prevalence and clinical profile of troponin T mutations among patients with hypertrophic cardiomyopathy in Tuscany
    • Torricelli F., Girolami F., Olivotto I., Passerini I., Frusconi S., Vargiu D., et al. Prevalence and clinical profile of troponin T mutations among patients with hypertrophic cardiomyopathy in Tuscany. Am J Cardiol 92 (2003) 1358-1362
    • (2003) Am J Cardiol , vol.92 , pp. 1358-1362
    • Torricelli, F.1    Girolami, F.2    Olivotto, I.3    Passerini, I.4    Frusconi, S.5    Vargiu, D.6
  • 6
    • 3142572751 scopus 로고    scopus 로고
    • Clinical features of hypertrophic cardiomyopathy caused by an Arg278Cys missense mutation in the cardiac troponin T gene
    • Theopistou A., Anastasakis A., Miliou A., Rigopoulos A., Toutouzas P., and Stefanadis C. Clinical features of hypertrophic cardiomyopathy caused by an Arg278Cys missense mutation in the cardiac troponin T gene. Am J Cardiol 94 (2004) 246-249
    • (2004) Am J Cardiol , vol.94 , pp. 246-249
    • Theopistou, A.1    Anastasakis, A.2    Miliou, A.3    Rigopoulos, A.4    Toutouzas, P.5    Stefanadis, C.6
  • 7
    • 0041866796 scopus 로고    scopus 로고
    • Hypertrophic cardiomyopathy: low frequency of mutations in the beta-myosin heavy chain (MYH7) and cardiac troponin T (TNNT2) genes among Spanish patients
    • García-Castro M., Reguero J.R., Batalla A., Díaz-Molina B., González P., Álvarez V., et al. Hypertrophic cardiomyopathy: low frequency of mutations in the beta-myosin heavy chain (MYH7) and cardiac troponin T (TNNT2) genes among Spanish patients. Clin Chem 49 (2003) 1279-1285
    • (2003) Clin Chem , vol.49 , pp. 1279-1285
    • García-Castro, M.1    Reguero, J.R.2    Batalla, A.3    Díaz-Molina, B.4    González, P.5    Álvarez, V.6
  • 8
    • 34548051735 scopus 로고    scopus 로고
    • Prevalence and spectrum of mutations in the sarcomeric troponin T and I genes in a cohort of Spanish cardiac hypertrophy patients
    • García-Castro M., Reguero J., Morís C., Alonso-Montes C., Berrazueta J.R., Sainz R., et al. Prevalence and spectrum of mutations in the sarcomeric troponin T and I genes in a cohort of Spanish cardiac hypertrophy patients. Int J Cardiol 121 (2007) 115-116
    • (2007) Int J Cardiol , vol.121 , pp. 115-116
    • García-Castro, M.1    Reguero, J.2    Morís, C.3    Alonso-Montes, C.4    Berrazueta, J.R.5    Sainz, R.6
  • 9
    • 59749096283 scopus 로고    scopus 로고
    • Espectro mutacional de los genes sarcoméricos MYH7, MYBPC3, TNNT2, TNNI3 y TPM1 en pacientes con miocardiopatía hipertrófica
    • García-Castro M., Coto E., Reguero J.R., Berrazueta J.R., Alvarez V., Alonso B., et al. Espectro mutacional de los genes sarcoméricos MYH7, MYBPC3, TNNT2, TNNI3 y TPM1 en pacientes con miocardiopatía hipertrófica. Rev Esp Cardiol 62 (2009) 48-56
    • (2009) Rev Esp Cardiol , vol.62 , pp. 48-56
    • García-Castro, M.1    Coto, E.2    Reguero, J.R.3    Berrazueta, J.R.4    Alvarez, V.5    Alonso, B.6
  • 10
    • 0025279744 scopus 로고
    • Hypertrophic cardiomyopathy without hypertrophy: two families with myocardial disarray in the absence of increased myocardial mass
    • McKenna W.J., Stewart J.T., Nihoyannopoulos P., McGinty F., and Davies M.J. Hypertrophic cardiomyopathy without hypertrophy: two families with myocardial disarray in the absence of increased myocardial mass. Br Heart J 63 (1990) 287-290
    • (1990) Br Heart J , vol.63 , pp. 287-290
    • McKenna, W.J.1    Stewart, J.T.2    Nihoyannopoulos, P.3    McGinty, F.4    Davies, M.J.5
  • 12
    • 0032483037 scopus 로고    scopus 로고
    • 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
    • Anan R., Shono H., Kisanuki A., Arima S., Nakao S., and Tanaka H. 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. Circulation 98 (1998) 391-397
    • (1998) Circulation , vol.98 , pp. 391-397
    • Anan, R.1    Shono, H.2    Kisanuki, A.3    Arima, S.4    Nakao, S.5    Tanaka, H.6
  • 13
    • 0034680324 scopus 로고    scopus 로고
    • Homozygous mutation in cardiac troponin T. Implications for hypertrophic cardiomyopathy
    • Ho C.Y., Lever H.M., DeSanctis R., Farver C.F., Seidman J.C., and Seidman C.E. Homozygous mutation in cardiac troponin T. Implications for hypertrophic cardiomyopathy. Circulation 102 (2000) 1950-1955
    • (2000) Circulation , vol.102 , pp. 1950-1955
    • Ho, C.Y.1    Lever, H.M.2    DeSanctis, R.3    Farver, C.F.4    Seidman, J.C.5    Seidman, C.E.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.