Identification of the haplotype associated with the APOB-3500 mutation in a French hypercholesterolemic subject: further support for a unique European ancestral mutation

Hum Mutat. 1993;2(2):145-7. doi: 10.1002/humu.1380020216.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Apolipoproteins B / genetics
  • Base Sequence
  • DNA / genetics
  • DNA Mutational Analysis
  • Europe
  • Female
  • France
  • Genetic Markers
  • Haplotypes / genetics*
  • Humans
  • Hyperlipoproteinemia Type II / blood
  • Hyperlipoproteinemia Type II / genetics*
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Mutation*
  • Pedigree

Substances

  • Apolipoproteins B
  • Genetic Markers
  • DNA