A Novel Mutation in KVLQT1 Is the Molecular Basis of Inherited Long QT Syndrome in a Near-Drowning Patient's Family
Open Access
- 1 August 1998
- journal article
- case report
- Published by Springer Nature in Pediatric Research
- Vol. 44 (2) , 148-153
- https://doi.org/10.1203/00006450-199808000-00002
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- The Long QT Syndrome: Ion Channel Diseases of the HeartMayo Clinic Proceedings, 1998
- Identification of a Family With Inherited Long QT Syndrome After a Pediatric Near-drowningPediatrics, 1998
- Ion Channels — Basic Science and Clinical DiseaseNew England Journal of Medicine, 1997
- Differential Response to Na + Channel Blockade, β-Adrenergic Stimulation, and Rapid Pacing in a Cellular Model Mimicking the SCN5A and HERG Defects Present in the Long-QT SyndromeCirculation Research, 1996
- Long QT Syndrome Patients With Mutations of the SCN5A and HERG Genes Have Differential Responses to Na + Channel Blockade and to Increases in Heart RateCirculation, 1995
- ECG T-Wave Patterns in Genetically Distinct Forms of the Hereditary Long QT SyndromeCirculation, 1995
- Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneityNature Genetics, 1994
- Linkage of a Cardiac Arrhythmia, the Long QT Syndrome, and the Harvey ras -1 GeneScience, 1991
- 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