677→CT mutation on the methylenetetrahydrofolate reductase gene is not a risk factor for neural tube defects in Turkey

Samankaltaisia teoksia

• Methylenetetrahydrofolate reductase mutations, a genetic cause for familial recurrent neural tube defects
  Tekijä: Yaliwal, Laxmi V., et al.
  Julkaistu: (2012)
• A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?
  Tekijä: van der Put, N M, et al.
  Julkaistu: (1998)
• Comorbidity of 5,10-methylenetetrahydrofolate reductase and methionine synthase gene polymorphisms and risk for neural tube defects
  Tekijä: JOHANNING, G., et al.
  Julkaistu: (2000)
• Examinations of Methylenetetrahydrofolate Reductase C677T and A1298C Mutations—and In Utero Viability
  Tekijä: Volcik, K. A., et al.
  Julkaistu: (2001)
• Heterogeneity in world distribution of the thermolabile C677T mutation in 5,10-methylenetetrahydrofolate reductase.
  Tekijä: Pepe, G, et al.
  Julkaistu: (1998)