Novel mutations in domain I of SCN5A cause Brugada syndrome
- 1 April 2002
- journal article
- Published by Elsevier in Molecular Genetics and Metabolism
- Vol. 75 (4) , 317-324
- https://doi.org/10.1016/s1096-7192(02)00006-9
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome: A multicenter reportPublished by Elsevier ,2010
- Cardiac conduction defects associate with mutations in SCN5ANature Genetics, 1999
- Ion channels and ventricular arrhythmias: cellular and ionic mechanisms underlying the Brugada syndromeCurrent Opinion in Cardiology, 1999
- The Brugada syndrome: clinical, electrophysiologic and genetic aspectsJournal of the American College of Cardiology, 1999
- Genetic basis and molecular mechanism for idiopathic ventricular fibrillationNature, 1998
- Arrhythmogenic Marker for the Sudden Unexplained Death Syndrome in Thai MenCirculation, 1997
- Further Characterization of the Syndrome of Right Bundle Branch Block, ST Segment Elevation, and Sudden Cardiac DeathJournal of Cardiovascular Electrophysiology, 1997
- Multiple Mechanisms of Na + Channel– Linked Long-QT SyndromeCirculation Research, 1996
- Molecular mechanism for an inherited cardiac arrhythmiaNature, 1995
- SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndromeCell, 1995