Gene-Specific Therapy for Long QT Syndrome.
- 1 July 1997
- journal article
- Published by Wiley in Annals of Noninvasive Electrocardiology
- Vol. 2 (3) , 274-278
- https://doi.org/10.1111/j.1542-474x.1997.tb00336.x
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Coassembly of KVLQT1 and minK (IsK) proteins to form cardiac IKS potassium channelNature, 1996
- Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmiasNature Genetics, 1996
- ECG T-Wave Patterns in Genetically Distinct Forms of the Hereditary Long QT SyndromeCirculation, 1995
- Molecular mechanism for an inherited cardiac arrhythmiaNature, 1995
- 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
- Evidence of genetic heterogeneity in Romano-Ward long QT syndrome. Analysis of 23 families.Circulation, 1994
- Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneityNature Genetics, 1994
- The long QT syndrome. Prospective longitudinal study of 328 families.Circulation, 1991
- Linkage of a Cardiac Arrhythmia, the Long QT Syndrome, and the Harvey ras -1 GeneScience, 1991