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