Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing
Top Cited Papers
- 6 April 2005
- journal article
- Published by Elsevier in Heart Rhythm
- Vol. 2 (5), 507-517
- https://doi.org/10.1016/j.hrthm.2005.01.020
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: Implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testingHeart Rhythm, 2004
- Spectrum and Frequency of Cardiac Channel Defects in Swimming-Triggered Arrhythmia SyndromesCirculation, 2004
- Ethnic Differences in Cardiac Potassium Channel Variants: Implications for Genetic Susceptibility to Sudden Cardiac Death and Genetic Testing for Congenital Long QT SyndromeMayo Clinic Proceedings, 2003
- Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac deathNature, 2003
- Epinephrine-Induced QT Interval Prolongation: A Gene-Specific Paradoxical Response in Congenital Long QT SyndromeMayo Clinic Proceedings, 2002
- Genomic Structure of Three Long QT Syndrome Genes:KVLQT1, HERG,andKCNE1Genomics, 1998
- The Long QT Syndrome: Ion Channel Diseases of the HeartMayo Clinic Proceedings, 1998
- SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndromeCell, 1995
- A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndromeCell, 1995
- Linkage of a Cardiac Arrhythmia, the Long QT Syndrome, and the Harvey ras -1 GeneScience, 1991