Spina bifida and common mutations at the homocysteine metabolism pathway

Clin Genet. 2000 Mar;57(3):230-1. doi: 10.1034/j.1399-0004.2000.570310.x.
No abstract available

Publication types

  • Letter

MeSH terms

  • 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase / genetics
  • Alleles
  • Case-Control Studies
  • Cystathionine beta-Synthase / genetics
  • Female
  • Genotype
  • Homocysteine / genetics*
  • Homocysteine / metabolism*
  • Humans
  • Methylenetetrahydrofolate Reductase (NADPH2)
  • Mothers
  • Mutation*
  • Oxidoreductases Acting on CH-NH Group Donors / genetics
  • Risk
  • Spinal Dysraphism / genetics*
  • Vitamin B 12 / genetics

Substances

  • Homocysteine
  • Oxidoreductases Acting on CH-NH Group Donors
  • Methylenetetrahydrofolate Reductase (NADPH2)
  • 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase
  • Cystathionine beta-Synthase
  • Vitamin B 12