A molecular and clinical study of heterozygous familial hyplercholesterolemia in the Finnish North Karelia

Scand Cardiovasc J. 1999;33(4):252-3. doi: 10.1080/14017439950141722.
No abstract available

MeSH terms

  • Adult
  • Apolipoproteins E / genetics
  • Female
  • Finland / epidemiology
  • Gene Deletion
  • Humans
  • Hyperlipoproteinemia Type II / epidemiology
  • Hyperlipoproteinemia Type II / genetics*
  • Infant, Newborn
  • Male
  • Middle Aged
  • Mutation
  • Polymorphism, Genetic
  • Receptors, LDL / genetics

Substances

  • Apolipoproteins E
  • Receptors, LDL