Homozygous C677T mutation of the 5,10 methylenetetrahydrofolate reductase gene and hyperhomocysteinemia in Italian patients with a history of early-onset ischemic stroke

Stroke. 1998 Apr;29(4):869-71. doi: 10.1161/01.str.29.4.869.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • 5,10-Methylenetetrahydrofolate Reductase (FADH2)
  • Adolescent
  • Adult
  • Age of Onset
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Female
  • Homocysteine / blood*
  • Homozygote*
  • Humans
  • Ischemic Attack, Transient / genetics*
  • Italy
  • Male
  • Methylenetetrahydrofolate Reductase (NADPH2)
  • Middle Aged
  • Mutation
  • Oxidoreductases / genetics*

Substances

  • Homocysteine
  • Oxidoreductases
  • 5,10-Methylenetetrahydrofolate Reductase (FADH2)
  • Methylenetetrahydrofolate Reductase (NADPH2)