Haplotype analysis in autosomal dominant polycystic kidney disease

J Med Genet. 1995 Mar;32(3):208-12. doi: 10.1136/jmg.32.3.208.

Abstract

Haplotype analysis was performed in 35 autosomal dominant polycystic kidney disease (ADPKD) families typed with 13 markers close to the PKD1 locus. The identification of recombinants close to the PKD1 gene on chromosome 16p indicates that PKD1 lies between CMM65 distally and 26-6 proximally. In addition, three unlinked (PKD2) families and two families with potential new mutation were identified.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Chromosomes, Human, Pair 16
  • Female
  • Genetic Linkage
  • Genetic Markers
  • Haplotypes / genetics*
  • Humans
  • Male
  • Middle Aged
  • Mutation
  • Polycystic Kidney, Autosomal Dominant / genetics*
  • Proteins / genetics
  • TRPP Cation Channels

Substances

  • Genetic Markers
  • Proteins
  • TRPP Cation Channels
  • polycystic kidney disease 1 protein