Retrospective Approach to Methylenetetrahydrofolate Reductase Mutations in Children

Author:

Özer Işıl,Özçetin Mustafa,Karaer Hatice,Kurt Semiha G.,Şahin Şemsettin

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference42 articles.

1. A common mutation in the metyhlenetetrahydrofolate reductase gene is associated with an accumulation of formylated tetrahydrofolates in red blood cells;Bagley;Med Sci,1998

2. Genomic structure and transcript variants of the human methylenetetrahydrofolate reductase gene;Homberger;Eur J Hum Genet,2000

3. A second genetic polymorphism in metyhlenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity;Weisberg;Mol Genet Metab,1998

4. Conversion of 5-formyltetrahydrofolic acid is unimpaired in folate-adequate persons homozygous for the C677T mutation in themethylenetetrahydrofolate reductase gene;Stern;J Nutr,2000

5. A common polymorphism in the methylenetetrahydrofolat reductase gene, homocysteine, and ischemic cerebrovascular disease;Markus;Stroke,1997

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