Evaluation of genetic variants in the reduced folate carrier and in glutamate carboxypeptidase II for spina bifida risk
- 11 June 2003
- journal article
- Published by Elsevier in Molecular Genetics and Metabolism
- Vol. 79 (3) , 197-200
- https://doi.org/10.1016/s1096-7192(03)00086-6
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Studies with His475Tyr glutamate carboxipeptidase II polymorphism and neural tube defectsAmerican Journal of Medical Genetics, 2002
- Maternal periconceptional vitamin use, genetic variation of infant reduced folate carrier (A80G), and risk of spina bifidaAmerican Journal of Medical Genetics, 2002
- Glutamate carboxypeptidase II: a polymorphism associated with lower levels of serum folate and hyperhomocysteinemiaHuman Molecular Genetics, 2000
- A Polymorphism (80G->A) in the Reduced Folate Carrier Gene and Its Associations with Folate Status and HomocysteinemiaMolecular Genetics and Metabolism, 2000
- 5, 10-Methylenetetrahydrofolate Reductase Gene Variants and Congenital Anomalies: A HuGE ReviewAmerican Journal of Epidemiology, 2000
- A Common Variant in Methionine Synthase Reductase Combined with Low Cobalamin (Vitamin B12) Increases Risk for Spina BifidaMolecular Genetics and Metabolism, 1999
- Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defectsAmerican Journal of Medical Genetics, 1999
- Folate levels and neural tube defects. Implications for preventionJAMA, 1995
- Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifidaThe Lancet, 1995