MTHFR association with arteriosclerotic vascular disease?

Hum Genet. 1998 Jul;103(1):11-21. doi: 10.1007/s004390050776.

Abstract

Complex diseases are far more common than diseases that follow simple Mendelian patterns of inheritance. Difficulties are experienced in the designing of experiments to dissect out the contribution of a single allele to a complex phenotype. We review the literature regarding a point mutation in methylenetetrahydrofolate reductase, a candidate gene for susceptibility to vascular diseases.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Alleles
  • Arteriosclerosis / blood
  • Arteriosclerosis / genetics*
  • Databases, Bibliographic
  • Folic Acid / blood
  • Genetic Predisposition to Disease
  • Homocysteine / blood
  • Homozygote
  • Humans
  • MEDLINE
  • Methylenetetrahydrofolate Reductase (NADPH2)
  • Oxidoreductases Acting on CH-NH Group Donors / genetics*
  • Point Mutation*

Substances

  • Homocysteine
  • Folic Acid
  • Oxidoreductases Acting on CH-NH Group Donors
  • Methylenetetrahydrofolate Reductase (NADPH2)