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European Heart Journal 1999 20(16):1137-1139; doi:10.1053/euhj.1999.1511
Copyright © 1999 by the European Society of Cardiology.
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Editorial

Gene-specific lethality of arrhythmic events in the long QT syndrome? A message from the International Registry

1999, 1999

References

  1. Schwartz PJ, Periti M, Malliani A. The long Q-T syndrome. Am Heart J. 1975;89:378–390[CrossRef][ISI][Medline]
  2. Schwartz PJ. Idiopathic long QT syndrome: Progress and questions. Am Heart J. 1985;109:399–411[CrossRef][ISI][Medline]
  3. Wang Q, Shen J, Splawski I. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell. 1995;80:805–811[CrossRef][ISI][Medline]
  4. Curran ME, Splawski I, Timothy KW, Vincent GM, Green ED, Keating MT. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome. Cell. 1995;80:795–803[CrossRef][ISI][Medline]
  5. Wang Q, Curran ME, Splawski I. Positional cloning of a novel potassium channel gene: KvLQT1 mutations cause cardiac arrhythmias. Nat Genet. 1996;12:17–23[CrossRef][ISI][Medline]
  6. Neyroud N, Tesson F, Denjoy I. A novel mutation in the potassium channel gene KvLQT1 causes the Jervell and Lange–Nielsen cardioauditory syndrome. Nat Genet. 1997;15:186–189[CrossRef][ISI][Medline]
  7. Barhanin J, Lesage F, Guillemare E, Fink M, Lazdunski M, Romey G. KvLQT1 and IsK (minK) proteins associate to form the IKscardiac potassium current. Nature. 1996;384:78–80[CrossRef][Medline]
  8. Sanguinetti MC, Curran ME, Zou A. Coassembly of KvLQT1 and minK (IsK) proteins to form cardiac IKspotassium channel. Nature. 1996;384:80–83[CrossRef][Medline]
  9. Moss AJ, Zareba W, Benhorin J. ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome. Circulation. 1995;92:2929–2934[Abstract/Free Full Text]
  10. Schwartz PJ, Priori SG, Locati EH. Long QT syndrome patients with mutations on the SCN5A and HERG genes have differential responses to Na+channel blockade and to increases in heart rate. Implications for gene-specific therapy. Circulation. 1995;92:3381–3386[Abstract/Free Full Text]
  11. Bennett PB, Yazawa K, Makita N, George AL Jr. Molecular mechanism for an inherited cardiac arrhythmia. Nature. 1995;376:683–685[CrossRef][Medline]
  12. Dumaine R, Wang Q, Keating MT. Multiple mechanisms of Na+channel-linked long-QT syndrome. Circ Res. 1996;78:916–924[Abstract/Free Full Text]
  13. An RH, Bangalore R, Rosero SZ, Kass RS. Lidocaine block of LQT-3 mutant human Na+channels. Circ Res. 1996;79:103–108[Abstract/Free Full Text]
  14. Zareba W, Moss AJ, Schwartz PJ. Influence of the genotype on the clinical course of the Long QT Syndrome. N Engl J Med. 1998;339:960–965[Abstract/Free Full Text]
  15. Moss AJ, Schwartz PJ, Crampton RS. The long QT syndrome: prospective longitudinal study of 328 families. Circulation. 1991;84:1136–1144[Abstract/Free Full Text]
  16. Schwartz PJ. The idiopathic long QT syndrome: The need for a prospective registry. Eur Heart J. 1983;4:529–531[Abstract/Free Full Text]
  17. Shimizu W, Antzelevitch C. Cellular basis for the ECG features of the LQT1 form of the long QT syndrome. Effects of ß-adrenergic agonists and antagonists and sodium channel blockers on transmural dispersion of repolarization and Torsade de Pointes. Circulation. 1998;98:2314–2322[Abstract/Free Full Text]
  18. Schwartz, PJ, Priori, SG, Napolitano, C, Long QT syndrome, Zipes, DPJalife, J, Cardiac Electrophysiology. From cell to bedside, Philadelphia, WB Saunders Co.
  19. Vincent GM, Fox J, Zhang L, Timothy KW. Beta-blockers markedly reduce risk and syncope in KVLQT1 long QT patients. Circulation. 1996;94:I–204
  20. Priori, SG, Napolitano, C, Schwartz, PJ, Low penetrance in the long QT syndrome. Clinical impact, Circulation
  21. Napolitano C, Priori SG, Schwartz PJ. Identification of a long QT syndrome molecular defect in drug-induced torsades de pointes. Circulation. 1997;96:211
  22. An RH, Wang XL, Kerem B, Benhorin J, Medina A, Goldmit M, Kass RS. Novel LQT-3 mutation affects Na+channel activity through interactions between {alpha}- and ß1-subunits. Circ Res. 1998;83:141–146[Abstract/Free Full Text]
  23. Chen Q, Kirsch GE, Zhang D. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. Nature. 1998;392:293–296[CrossRef][Medline]

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