A new APOA1 mutation with severe HDL-cholesterol deficiency and premature coronary artery disease

Clin Chim Acta. 2008 Feb;388(1-2):222-4. doi: 10.1016/j.cca.2007.10.015. Epub 2007 Oct 17.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Apolipoprotein A-I / genetics*
  • Coronary Artery Disease / genetics*
  • Coronary Artery Disease / pathology*
  • Female
  • Humans
  • Hypoalphalipoproteinemias / genetics*
  • Hypoalphalipoproteinemias / pathology*
  • Male
  • Middle Aged
  • Mutation / genetics
  • Pedigree

Substances

  • APOA1 protein, human
  • Apolipoprotein A-I