메뉴 건너뛰기




Volumn 34, Issue 7, 1999, Pages 2035-2042

Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts

Author keywords

[No Author keywords available]

Indexed keywords

FLECAINIDE;

EID: 0033405388     PISSN: 07351097     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0735-1097(99)00461-1     Document Type: Article
Times cited : (305)

References (52)
  • 1
    • 0026759352 scopus 로고
    • The spectrum of symptoms and QT intervals in carriers of the gene for the long QT syndrome
    • Vincent G.M., Timothy K.W., Leppert M., Keating M. The spectrum of symptoms and QT intervals in carriers of the gene for the long QT syndrome. N Engl J Med. 327:1992;846-852.
    • (1992) N Engl J Med , vol.327 , pp. 846-852
    • Vincent, G.M.1    Timothy, K.W.2    Leppert, M.3    Keating, M.4
  • 2
    • 0023848617 scopus 로고
    • Right ventricular cardiomyopathy and sudden death in young people
    • Thiene G., Nava A., Corrado D., Rossi L., Pennelli N. Right ventricular cardiomyopathy and sudden death in young people. N Engl J Med. 318:1988;129-133.
    • (1988) N Engl J Med , vol.318 , pp. 129-133
    • Thiene, G.1    Nava, A.2    Corrado, D.3    Rossi, L.4    Pennelli, N.5
  • 3
    • 0028902929 scopus 로고
    • Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy
    • Watkins H., McKenna W.J., Thierfelder L., 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
  • 4
    • 0031978985 scopus 로고    scopus 로고
    • The molecular genetics of the long QT syndrome: Genes causing fainting and sudden death
    • Vincent G.M. The molecular genetics of the long QT syndrome genes causing fainting and sudden death . Annu Rev Med. 49:1998;263-274.
    • (1998) Annu Rev Med , vol.49 , pp. 263-274
    • Vincent, G.M.1
  • 5
    • 0029020780 scopus 로고
    • Right ventricular dysplasia: The Mayo Clinic experience
    • Kullo I.J., Edwards W.D., Seward J.B. Right ventricular dysplasia the Mayo Clinic experience . Mayo Clin Proc. 70:1995;541-548.
    • (1995) Mayo Clin Proc , vol.70 , pp. 541-548
    • Kullo, I.J.1    Edwards, W.D.2    Seward, J.B.3
  • 6
    • 0030712343 scopus 로고    scopus 로고
    • Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: A multicenter study
    • Corrado D., Basso C., Thiene G., et al. Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia a multicenter study . J Am Coll Cardiol. 30:1997;1512-1520.
    • (1997) J Am Coll Cardiol , vol.30 , pp. 1512-1520
    • Corrado, D.1    Basso, C.2    Thiene, G.3
  • 7
    • 0028807911 scopus 로고
    • A new locus for arrhythmogenic right ventricular cardiomyopathy (ARVD2) maps to chromosome 1q42-q43
    • Rampazzo A., Nava A., Erne P., et al. A new locus for arrhythmogenic right ventricular cardiomyopathy (ARVD2) maps to chromosome 1q42-q43. Hum Mol Genetics. 4:1995;2151-2154.
    • (1995) Hum Mol Genetics , vol.4 , pp. 2151-2154
    • Rampazzo, A.1    Nava, A.2    Erne, P.3
  • 8
    • 0030724006 scopus 로고    scopus 로고
    • ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm
    • Rampazzo A., Nava A., Miorin M., et al. ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm. Genomics. 45:1997;259-263.
    • (1997) Genomics , vol.45 , pp. 259-263
    • Rampazzo, A.1    Nava, A.2    Miorin, M.3
  • 9
    • 0028243281 scopus 로고
    • The gene for arrhythmogenic right ventricular cardiomyopathy maps to chromosome 14q23-q24
    • Rampazzo A., Nava A., Buja G., et al. The gene for arrhythmogenic right ventricular cardiomyopathy maps to chromosome 14q23-q24. Hum Mol Genetics. 3:1994;959-962.
    • (1994) Hum Mol Genetics , vol.3 , pp. 959-962
    • Rampazzo, A.1    Nava, A.2    Buja, G.3
  • 10
    • 0030050430 scopus 로고    scopus 로고
    • A new locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14
    • Severini G.M., Krajinovic M., Pinamonti B., et al. A new locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14. Genomics. 31:1996;193-200.
    • (1996) Genomics , vol.31 , pp. 193-200
    • Severini, G.M.1    Krajinovic, M.2    Pinamonti, B.3
  • 11
    • 0032578962 scopus 로고    scopus 로고
    • Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23
    • Ahmad F., Duanxiang L., Karibe A., et al. Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23. Circulation. 98:1998;2791-2795.
    • (1998) Circulation , vol.98 , pp. 2791-2795
    • Ahmad, F.1    Duanxiang, L.2    Karibe, A.3
  • 12
    • 0001127258 scopus 로고
    • An analysis of the time-relations of electrocardiograms
    • Bazett H.C. An analysis of the time-relations of electrocardiograms. Heart. 7:1920;353-370.
    • (1920) Heart , vol.7 , pp. 353-370
    • Bazett, H.C.1
  • 13
    • 0019975195 scopus 로고
    • Ventricular activation during ventricular endocardial pacing. I. Electrocardiographic patterns related to the site of pacing
    • Waxman H.L., Josephson M.E. Ventricular activation during ventricular endocardial pacing. I. Electrocardiographic patterns related to the site of pacing. Am J Cardiol. 50:1982;1-10.
    • (1982) Am J Cardiol , vol.50 , pp. 1-10
    • Waxman, H.L.1    Josephson, M.E.2
  • 14
    • 0019431045 scopus 로고
    • Identification of patients with ventricular tachycardia after myocardial infarction from signals in the terminal QRS complex
    • Simson M.B. Identification of patients with ventricular tachycardia after myocardial infarction from signals in the terminal QRS complex. Circulation. 64:1981;235-242.
    • (1981) Circulation , vol.64 , pp. 235-242
    • Simson, M.B.1
  • 15
    • 0026466921 scopus 로고
    • Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome. A multicenter report
    • Brugada P., Brugada J. Right bundle branch block, persistent ST segment elevation and sudden cardiac death a distinct clinical and electrocardiographic syndrome. A multicenter report . J Am Coll Cardiol. 20:1992;1391-1396.
    • (1992) J Am Coll Cardiol , vol.20 , pp. 1391-1396
    • Brugada, P.1    Brugada, J.2
  • 17
    • 0025124993 scopus 로고
    • Diagnostic accuracy of right ventriculography in arrhythmogenic right ventricular cardiomyopathy
    • Daliento L., Rizzoli G., Thiene G., et al. Diagnostic accuracy of right ventriculography in arrhythmogenic right ventricular cardiomyopathy. Am J Cardiol. 66:1990;741-745.
    • (1990) Am J Cardiol , vol.66 , pp. 741-745
    • Daliento, L.1    Rizzoli, G.2    Thiene, G.3
  • 18
    • 0016708084 scopus 로고
    • Right ventricular performance in patients with coronary artery disease
    • Ferlinz J., Gorlin R., Cohn P.F., Herman M.V. Right ventricular performance in patients with coronary artery disease. Circulation. 52:1975;608-615.
    • (1975) Circulation , vol.52 , pp. 608-615
    • Ferlinz, J.1    Gorlin, R.2    Cohn, P.F.3    Herman, M.V.4
  • 19
    • 13344259999 scopus 로고    scopus 로고
    • A comprehensive genetic map of the human genome based on 5,264 microsatellites
    • Dib C., Fauré S., Fizames C., et al. A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature. 380:1996;152-154.
    • (1996) Nature , vol.380 , pp. 152-154
    • Dib, C.1    Fauré, S.2    Fizames, C.3
  • 23
    • 0029886532 scopus 로고    scopus 로고
    • Parametric and nonparametric linkage analysis: A unified multipoint approach
    • Kruglyak L., Daly M.J., Reeve-Daly M.P., Lander E.S. Parametric and nonparametric linkage analysis a unified multipoint approach . Am J Hum Genetics. 58:1996;1347-1363.
    • (1996) Am J Hum Genetics , vol.58 , pp. 1347-1363
    • Kruglyak, L.1    Daly, M.J.2    Reeve-Daly, M.P.3    Lander, E.S.4
  • 24
    • 0022792421 scopus 로고
    • Estimating the power of a proposed linkage study: A practical computer simulation approach
    • Boehnke M. Estimating the power of a proposed linkage study a practical computer simulation approach . Am J Hum Genetics. 39:1986;513-527.
    • (1986) Am J Hum Genetics , vol.39 , pp. 513-527
    • Boehnke, M.1
  • 25
    • 0024602536 scopus 로고
    • Estimating the power of a proposed linkage study for a complex genetic trait
    • Ploughman L.M., Boehnke M. Estimating the power of a proposed linkage study for a complex genetic trait. Am J Hum Genetics. 44:1989;543-551.
    • (1989) Am J Hum Genetics , vol.44 , pp. 543-551
    • Ploughman, L.M.1    Boehnke, M.2
  • 26
    • 0029871919 scopus 로고    scopus 로고
    • TWIK-1, a ubiquitous human weakly inward rectifying K+ channel with a novel structure
    • Lesage F., Guillemare E., Fink M., et al. TWIK-1, a ubiquitous human weakly inward rectifying K+ channel with a novel structure. EMBO J. 15:1996;1004-1011.
    • (1996) EMBO J , vol.15 , pp. 1004-1011
    • Lesage, F.1    Guillemare, E.2    Fink, M.3
  • 28
    • 0028819671 scopus 로고
    • Mapping of a gene for long QT syndrome to chromosome 4q25-27
    • Schott J.J., Charpentier F., Peltier S., et al. Mapping of a gene for long QT syndrome to chromosome 4q25-27. Am J Hum Genetics. 57:1995;1114-1122.
    • (1995) Am J Hum Genetics , vol.57 , pp. 1114-1122
    • Schott, J.J.1    Charpentier, F.2    Peltier, S.3
  • 29
    • 9044240040 scopus 로고    scopus 로고
    • Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
    • Wang Q., Curran M.E., Splawski I., et al. Positional cloning of a novel potassium channel gene KVLQT1 mutations cause cardiac arrhythmias . Nat Genetics. 12:1996;17-23.
    • (1996) Nat Genetics , vol.12 , pp. 17-23
    • Wang, Q.1    Curran, M.E.2    Splawski, I.3
  • 30
    • 0029992905 scopus 로고    scopus 로고
    • Genomic organization of the human SCN5A gene encoding the cardiac sodium channel
    • Wang Q., Curran M.E., Splawski I., et al. Genomic organization of the human SCN5A gene encoding the cardiac sodium channel. Genomics. 34:1996;9-16.
    • (1996) Genomics , vol.34 , pp. 9-16
    • Wang, Q.1    Curran, M.E.2    Splawski, I.3
  • 31
    • 0024309922 scopus 로고
    • Molecular cloning and sequence analysis of a human genomic DNA encoding a novel membrane protein which exhibits a slow activating potassium channel activity
    • Murai T., Kazikuka A., Takumi T., Ohkubo H., Nakanishi S. Molecular cloning and sequence analysis of a human genomic DNA encoding a novel membrane protein which exhibits a slow activating potassium channel activity. Biochem Biophys Res Commun. 161:1989;176-181.
    • (1989) Biochem Biophys Res Commun , vol.161 , pp. 176-181
    • Murai, T.1    Kazikuka, A.2    Takumi, T.3    Ohkubo, H.4    Nakanishi, S.5
  • 32
    • 0023734276 scopus 로고
    • Cloning of a membrane protein that induces a slow voltage-gated potassium current
    • Takumi T., Ohkubo H., Nakanishi S. Cloning of a membrane protein that induces a slow voltage-gated potassium current. Science. 242:1988;1042-1045.
    • (1988) Science , vol.242 , pp. 1042-1045
    • Takumi, T.1    Ohkubo, H.2    Nakanishi, S.3
  • 33
    • 0029937123 scopus 로고    scopus 로고
    • Assignment of human weak inward rectifier K+ channel TWIK-1 gene to chromosome 1q42-q43
    • Lesage F., Mattéi M.-G., Fink M., Barhanin J., Lazdunski M. Assignment of human weak inward rectifier K+ channel TWIK-1 gene to chromosome 1q42-q43. Genomics. 34:1996;153-155.
    • (1996) Genomics , vol.34 , pp. 153-155
    • Lesage, F.1    Mattéi, M.-G.2    Fink, M.3    Barhanin, J.4    Lazdunski, M.5
  • 34
    • 0030992683 scopus 로고    scopus 로고
    • The molecular genetics of hypertrophic cardiomyopathy
    • Malik M.S., Watkins H. The molecular genetics of hypertrophic cardiomyopathy. Curr Opin Cardiol. 12:1997;295-302.
    • (1997) Curr Opin Cardiol , vol.12 , pp. 295-302
    • Malik, M.S.1    Watkins, H.2
  • 35
    • 0028145745 scopus 로고
    • A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1
    • Kass S., MacRae C., Graber H.L., et al. A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1. Nat Genetics. 7:1994;546-551.
    • (1994) Nat Genetics , vol.7 , pp. 546-551
    • Kass, S.1    MacRae, C.2    Graber, H.L.3
  • 36
    • 0028801254 scopus 로고
    • Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32
    • Durand J.B., Bachinski L.L., Bieling L.C., et al. Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32. Circulation. 92:1995;3387-3389.
    • (1995) Circulation , vol.92 , pp. 3387-3389
    • Durand, J.B.1    Bachinski, L.L.2    Bieling, L.C.3
  • 37
    • 0030882270 scopus 로고    scopus 로고
    • Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23
    • Messina D.N., Speer M.C., Pericak-Vance M.A., McNally E.M. Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23. Am J Hum Genetics. 61:1997;909-917.
    • (1997) Am J Hum Genetics , vol.61 , pp. 909-917
    • Messina, D.N.1    Speer, M.C.2    Pericak-Vance, M.A.3    McNally, E.M.4
  • 38
    • 0029151478 scopus 로고
    • Linkage of familial dilated cardiomyopathy to chromosome 9. Heart Muscle Disease Study Group
    • Krajinovic M., Pinamonti B., Sinagra G., et al. Linkage of familial dilated cardiomyopathy to chromosome 9. Heart Muscle Disease Study Group. Am J Hum Genetics. 57:1995;846-852.
    • (1995) Am J Hum Genetics , vol.57 , pp. 846-852
    • Krajinovic, M.1    Pinamonti, B.2    Sinagra, G.3
  • 39
    • 0029784361 scopus 로고    scopus 로고
    • Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23
    • Bowles K.R., Gajarski R., Porter P., et al. Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23. J Clin Invest. 98:1996;1355-1360.
    • (1996) J Clin Invest , vol.98 , pp. 1355-1360
    • Bowles, K.R.1    Gajarski, R.2    Porter, P.3
  • 40
    • 0032076955 scopus 로고    scopus 로고
    • Actin mutations in dilated cardiomyopathy, a heritable form of heart failure
    • Olson T.M., Michels V.V., Thibodeau S.N., Tai Y.-S., Keating M.T. Actin mutations in dilated cardiomyopathy, a heritable form of heart failure. Science. 280:1998;750-752.
    • (1998) Science , vol.280 , pp. 750-752
    • Olson, T.M.1    Michels, V.V.2    Thibodeau, S.N.3    Tai, Y.-S.4    Keating, M.T.5
  • 41
    • 0027193330 scopus 로고
    • X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus
    • Towbin J.A., Hejtmancik J.F., Brink P., et al. X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus. Circulation. 87:1993;1854-1865.
    • (1993) Circulation , vol.87 , pp. 1854-1865
    • Towbin, J.A.1    Hejtmancik, J.F.2    Brink, P.3
  • 42
    • 14444268277 scopus 로고    scopus 로고
    • Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy
    • Muntoni F., Di Lenarda A., Porcu M., et al. Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy. Heart. 78:1997;608-612.
    • (1997) Heart , vol.78 , pp. 608-612
    • Muntoni, F.1    Di Lenarda, A.2    Porcu, M.3
  • 43
    • 0025807222 scopus 로고
    • Maternally inherited myopathy and cardiomyopathy: Association with mutation in mitochondrial DNA tRNA(Leu) (UUR)
    • Zeviani M., Gellera C., Antozzi C., et al. Maternally inherited myopathy and cardiomyopathy association with mutation in mitochondrial DNA tRNA(Leu) (UUR) . Lancet. 338:1991;143-147.
    • (1991) Lancet , vol.338 , pp. 143-147
    • Zeviani, M.1    Gellera, C.2    Antozzi, C.3
  • 44
    • 0032546384 scopus 로고    scopus 로고
    • Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
    • Chen Q.Y., Kirsch G.E., Zhang D.M., et al. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. Nature. 392:1998;293-296.
    • (1998) Nature , vol.392 , pp. 293-296
    • Chen, Q.Y.1    Kirsch, G.E.2    Zhang, D.M.3
  • 45
    • 0028347223 scopus 로고
    • Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy
    • McKenna W.J., Thiene G., Nava A., et al. Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Br Heart J. 71:1994;215-218.
    • (1994) Br Heart J , vol.71 , pp. 215-218
    • McKenna, W.J.1    Thiene, G.2    Nava, A.3
  • 46
    • 0032574651 scopus 로고
    • Arrhythmogenic right ventricular cardiomyopathy and fatty replacement of the right ventricular myocardium. Are they different diseases?
    • Burke A.P., Farb A., Tashko G., Virmani R. Arrhythmogenic right ventricular cardiomyopathy and fatty replacement of the right ventricular myocardium. Are they different diseases? Circulation. 97:1988;1571-1580.
    • (1988) Circulation , vol.97 , pp. 1571-1580
    • Burke, A.P.1    Farb, A.2    Tashko, G.3    Virmani, R.4
  • 48
    • 0030246848 scopus 로고    scopus 로고
    • Value of quantitative measurement of signal-averaged electrocardiographic variables in arrhythmogenic right ventricular dysplasia: Correlation with echocardiographic right ventricular cavity dimensions
    • Mehta D., Goldman M., David O., Gomes J.A. Value of quantitative measurement of signal-averaged electrocardiographic variables in arrhythmogenic right ventricular dysplasia correlation with echocardiographic right ventricular cavity dimensions . J Am Coll Cardiol. 28:1996;713-719.
    • (1996) J Am Coll Cardiol , vol.28 , pp. 713-719
    • Mehta, D.1    Goldman, M.2    David, O.3    Gomes, J.A.4
  • 49
    • 0023694227 scopus 로고
    • Juvenile sudden death and effort ventricular tachycardias in a family with right ventricular cardiomyopathy
    • Nava A., Canciani B., Daliento L., et al. Juvenile sudden death and effort ventricular tachycardias in a family with right ventricular cardiomyopathy. Int J Cardiol. 21:1988;111-123.
    • (1988) Int J Cardiol , vol.21 , pp. 111-123
    • Nava, A.1    Canciani, B.2    Daliento, L.3
  • 50
    • 0016662531 scopus 로고
    • Bidirectional tachycardia in a child. A study using His bundle electrography
    • Reid D.S., Tynan M., Braidwood L., Fitzgerald G.R. Bidirectional tachycardia in a child. A study using His bundle electrography. Br Heart J. 37:1975;339-344.
    • (1975) Br Heart J , vol.37 , pp. 339-344
    • Reid, D.S.1    Tynan, M.2    Braidwood, L.3    Fitzgerald, G.R.4
  • 51
    • 0028957403 scopus 로고
    • Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients
    • Leenhardt A., Lucet V., Denjoy I., Grau F., Ngoc D.D., Coumel P. Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients. Circulation. 91:1995;1512-1519.
    • (1995) Circulation , vol.91 , pp. 1512-1519
    • Leenhardt, A.1    Lucet, V.2    Denjoy, I.3    Grau, F.4    Ngoc, D.D.5    Coumel, P.6
  • 52
    • 0029815650 scopus 로고    scopus 로고
    • The human cardiac muscle ryanodine receptor-calcium release channel: Identification, primary structure and topological analysis
    • Tunwell R.E., Wickenden C., Bertrand B.M., et al. The human cardiac muscle ryanodine receptor-calcium release channel identification, primary structure and topological analysis . Biochem J. 318:1996;477-487.
    • (1996) Biochem J , vol.318 , pp. 477-487
    • Tunwell, R.E.1    Wickenden, C.2    Bertrand, B.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.