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Volumn 115, Issue 4, 2010, Pages 311-316

Sick sinus syndrome, progressive cardiac conduction disease, atrial flutter and ventricular tachycardia caused by a novel SCN5A mutation

Author keywords

Atrial fibrillation; Brugada syndrome; Overlapping phenotypes; SCN5A; Sick sinus syndrome; Ventricular tachycardia

Indexed keywords

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EID: 77950826491     PISSN: 00086312     EISSN: None     Source Type: Journal    
DOI: 10.1159/000312747     Document Type: Article
Times cited : (19)

References (9)
  • 1
    • 33646769244 scopus 로고    scopus 로고
    • Highefficiency multiplex capillary electrophoresis single strand conformation polymorphism (multi-CE-SSCP) mutation screening of SCN5A: A rapid genetic approach to cardiac arrhythmia
    • Hofman-Bang J, Behr ER, Hedley P, Tfelt-Hansen J, Kanters JK, Haunsoe S, et al: Highefficiency multiplex capillary electrophoresis single strand conformation polymorphism (multi-CE-SSCP) mutation screening of SCN5A: a rapid genetic approach to cardiac arrhythmia. Clin Genet 2006; 69: 504-511.
    • (2006) Clin. Genet. , vol.69 , pp. 504-511
    • Hofman-Bang, J.1    Behr, E.R.2    Hedley, P.3    Tfelt-Hansen, J.4    Kanters, J.K.5    Haunsoe, S.6
  • 4
    • 13444300924 scopus 로고    scopus 로고
    • Brugada syndrome: Report of the second consensus conference: Endorsed by the Heart Rhythm Society and the European Heart Rhythm Association
    • Antzelevitch C, Brugada P, Borggrefe M, Brugada J, Brugada R, Corrado D, et al: Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association. Circulation 2005; 111: 659-670.
    • (2005) Circulation , vol.111 , pp. 659-670
    • Antzelevitch, C.1    Brugada, P.2    Borggrefe, M.3    Brugada, J.4    Brugada, R.5    Corrado, D.6
  • 5
    • 33644761196 scopus 로고    scopus 로고
    • Progressive cardiac conduction defect is the prevailing phenotype in carriers of a Brugada syndrome SCN5A mutation
    • Probst V, Allouis M, Sacher F, Pattier S, Babuty D, Mabo P, et al: Progressive cardiac conduction defect is the prevailing phenotype in carriers of a Brugada syndrome SCN5A mutation. J Cardiovasc Electrophysiol 2006; 17: 270-275.
    • (2006) J. Cardiovasc. Electrophysiol. , vol.17 , pp. 270-275
    • Probst, V.1    Allouis, M.2    Sacher, F.3    Pattier, S.4    Babuty, D.5    Mabo, P.6
  • 6
    • 44449161964 scopus 로고    scopus 로고
    • Analyses of a novel SCN5A mutation (C1850S) : Conduction vs. repolarization disorder hypotheses in the Brugada syndrome
    • Petitprez S, Jespersen T, Pruvot E, Keller DI, Corbaz C, Schlapfer J, et al: Analyses of a novel SCN5A mutation (C1850S) : conduction vs. repolarization disorder hypotheses in the Brugada syndrome. Cardiovasc Res 2008; 78: 494-504.
    • (2008) Cardiovasc. Res. , vol.78 , pp. 494-504
    • Petitprez, S.1    Jespersen, T.2    Pruvot, E.3    Keller, D.I.4    Corbaz, C.5    Schlapfer, J.6
  • 7
    • 77449091606 scopus 로고    scopus 로고
    • SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome
    • Probst V, Wilde AA, Barc J, Sacher F, Babuty D, Mabo P, et al: SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome. Circ Cardiovasc Genet 2009; 2: 552-557.
    • (2009) Circ. Cardiovasc. Genet. , vol.2 , pp. 552-557
    • Probst, V.1    Wilde, A.A.2    Barc, J.3    Sacher, F.4    Babuty, D.5    Mabo, P.6
  • 8
    • 0037314358 scopus 로고    scopus 로고
    • A common SCN5A polymorphism modulates the biophysical effects of an SCN5A mutation
    • Viswanathan PC, Benson DW, Balser JR: A common SCN5A polymorphism modulates the biophysical effects of an SCN5A mutation. J Clin Invest 2003; 111: 341-346.
    • (2003) J. Clin. Invest. , vol.111 , pp. 341-346
    • Viswanathan, P.C.1    Benson, D.W.2    Balser, J.R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.