Readjusting the localization of long QT syndrome gene on chromosome 11p15

C R Acad Sci III. 1995 Aug;318(8):879-85.

Abstract

Long QT syndrome (LQT) is an autosomal dominant cardiac disease characterized by ventricular arrhythmia. A first locus for LQT has been identified on chromosome 11p15.5 (LQT1), closely linked to HRAS. To refine the location of LQT1, microsatellites were genotyped in 8 French families and the following order was determined: tel-HRAS-DRD4-D11S922-D11S4046- IGF2-INS-TH-D11S1318-D11S1323-D11S1338-D11S90 9-D11S1346-cen. By haplotype analysis, 12 crossing-over events were identified in affected and unaffected subjects, delineating the LQT1 candidate region to 7 cM. This new delineated localization between D11S1318 and D11S1323 is in a more centromeric region than previously thought and is 5 cM proximal to HRAS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosome Mapping
  • Chromosomes, Human, Pair 11 / genetics*
  • DNA, Satellite
  • Female
  • Genetic Markers
  • Haplotypes
  • Humans
  • Long QT Syndrome / genetics*
  • Male
  • Pedigree

Substances

  • DNA, Satellite
  • Genetic Markers