Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac death-Reference-Cited by-同舟云学术

Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac death

Published:2004-11 Issue:5 Volume:1 Page:610-615
ISSN:1547-5271
Container-title:Heart Rhythm
language:en
Short-container-title:Heart Rhythm

Author:

Rossenbacker Tom,Carroll Sheila J.,Liu Huajun,Kuipéri Cuno,de Ravel Thomy J.L.,Devriendt Koen,Carmeliet Peter,Kass Robert S.,Heidbüchel Hein

Publisher

Elsevier BV

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference18 articles.

1. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome;Wang;Cell,1995

2. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation;Chen;Nature,1998

3. Cardiac conduction defects associate with mutations in SCN5A;Schott;Nat Genet,1999

4. Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report;Brugada;J Am Coll Cardiol,1992

5. Genotype-phenotype relationship in Brugada syndrome;Smits;J Am Coll Cardiol,2002

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