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先天性长QT综合征相关突变基因

  3 Splawski 1,Tristani M,Lehmann MH,et al.Mutations in the hminK gene cause Long QCT syndrome and suppress IKs function.Nat Genet,1997,17(3):338~340.

  4 Roden DM,Balser JR,George AL,et al.Cardiac ion channels.Annu Rev Physiol, 2002,64(3):431~475.

  5 Anderson CL,Delisle BP,Anson BD,et al.Most LQT2 mutations reduce Kv11.1 (hERG) current by a class 2 (trafficking-deficient) mechanism.Circulation, 2006,113(3):365~373.

  6 Abott GW,Sesti F,Splawski I,et al.A common polymorphism associated with antibiotic induced cardiac arrhythmia. proc natl Sci,2000,97(19):10613~10618.

  7 Shin DJ,kim E,park SB,et al.A novel mutation in the SCN5A gene is associated with Brugada syndrome .Life Sci,2007,80(8):716~724.

  8 Argelia MD,Toshihiko Ka. SCN4B-Encoded Sodium Channel β4 Subunit in Congenital Long-QT Syndrome.Circulation,2007;116:134~142.

  9 Tamargo J,Caballero R,Gomez R,et al.Pharmacology of cardiac potassium channels.Cardiovasc Res,2004,62(1):9~33.

  10 Tristani Fi,Jensen JL,Donaldson MR,et al.Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome) .J Clin Invest, 2002,110(3):381~388.

  11 Wilde AA,Kb S.Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?.Eur Heart J,2007,28:575~580.

  12 Vyas H,Hejlik J,Ackerman MJ. Epinephrine QT stress testing in the evaluation of congenital long-QT syndrome:diagnostic accuracy of the paradoxical QT response.Circulation,2006,113:1385~1392.

  13 Sauer AJ,Moss AJ,McNitt S,et al.Long QT syndrome in adults .J Am Coll Cardiol, 2007,49:329~337.
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