Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene

Science. 1991 May 3;252(5006):704-6. doi: 10.1126/science.1673802.

Abstract

Genetic factors contribute to heart disease. In this study, linkage analyses have been performed in a family that is predisposed to sudden death from cardiac arrhythmias, the long QT syndrome (LQT). A DNA marker at the Harvey ras-1 locus (H-ras-1) was linked to LQT with a logarithm of the likelihood ratio for linkage (lod score) of 16.44 at theta = 0, which confirms the genetic basis of this trait and localizes this gene to the short arm of chromosome 11. As no recombination was observed between LQT and H-ras-1, and there is a physiological rationale for its involvement in this disease, ras becomes a candidate for the disease locus.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Chromosome Mapping
  • Chromosomes, Human, Pair 11
  • Electrocardiography
  • Genes, ras*
  • Humans
  • Lod Score*
  • Long QT Syndrome / genetics*
  • Long QT Syndrome / physiopathology
  • Mutation
  • Pedigree
  • Polymorphism, Restriction Fragment Length