Article
[Long QT syndrome].
Nihon rinsho. Japanese journal of clinical medicine - 1 Mar 1996
Nakajima T, Kaneko Y, Taniguchi Y, Nagai R
Abstract excerpt
Romano-Ward syndrome, one of familial long QT syndromes, is an inherited disorder that causes sudden death from cardiac arrhythmias, specifically torsade de pointes and ventricular fibrillation. By linkage analyses, three LQT loci were previously mapped: LQT1 on chromosome 11p15.5, LQT2 on 7q35-3...
Topics
- Animals
- Chromosome Mapping
- Humans
- Long QT Syndrome
- Mutation
- Potassium Channels
- Sodium Channels
