A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
- 1 March 1995
- Vol. 80 (5), 795-803
- https://doi.org/10.1016/0092-8674(95)90358-5
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- A human chromosome 7 yeast artificial chromosome (YAC) resource: construction, characterization, and screeningGenomics, 1995
- The 1993–94 Généthon human genetic linkage mapNature Genetics, 1994
- Integration of physical, genetic and cytogenetic maps of human chromosome 7: isolation and analysis of yeast artificial chromosome clones for 117 mapped genetic markersHuman Molecular Genetics, 1994
- Ether-à-go-go encodes a voltage-gated channel permeable to K+ and Ca2+ and modulated by cAMPNature, 1993
- The Spectrum of Symptoms and QT Intervals in Carriers of the Gene for the Long-QT SyndromeNew England Journal of Medicine, 1992
- Shaker, Shal, Shab, and Shaw express independent K+ current systemsNeuron, 1991
- Determination of the subunit stoichiometry of a voltage-activated potassium channelNature, 1991
- Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA librariesHuman Genetics, 1988
- Circadian variation in the incidence of sudden cardiac death in the framingham heart study populationThe American Journal of Cardiology, 1987
- Sudden death risk in overt coronary heart disease: The Framingham StudyAmerican Heart Journal, 1987