Frequency of delta F508 and haplotype association in Austrian cystic fibrosis families

Hum Genet. 1992 Jun;89(4):437-8. doi: 10.1007/BF00194318.

Abstract

The frequency of the major mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene was analyzed for 113 Austrian cystic fibrosis (CF) patients. An overall frequency of 55% for delta F508 was found with values of 72% and 13% for patients with pancreatic insufficiency (CF-PI) and those with pancreatic sufficiency (CF-PS), respectively. Furthermore, the distribution of the alleles of the closely linked DNA markers XV2c/KM19/MP6d-9 in our families is described.

MeSH terms

  • Austria
  • Cystic Fibrosis / genetics*
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Exocrine Pancreatic Insufficiency / genetics*
  • Gene Frequency / genetics*
  • Genetic Markers / genetics
  • Haplotypes
  • Humans
  • Membrane Proteins / genetics*
  • Mutation / genetics
  • Polymerase Chain Reaction
  • Polymorphism, Restriction Fragment Length

Substances

  • CFTR protein, human
  • Genetic Markers
  • Membrane Proteins
  • Cystic Fibrosis Transmembrane Conductance Regulator