Literature DB >> 10947212

Methylenetetrahydrofolate reductase 677C > T mutation and epilepsy.

H Ono1, A Sakamoto, N Mizoguchi, N Sakura.   

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Year:  2000        PMID： 10947212     DOI： 10.1023/a:1005680701884

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  2 in total

Review 1.  Molecular genetics of methylenetetrahydrofolate reductase deficiency.

Authors:  R Rozen
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

2.  A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase.

Authors:  P Frosst; H J Blom; R Milos; P Goyette; C A Sheppard; R G Matthews; G J Boers; M den Heijer; L A Kluijtmans; L P van den Heuvel
Journal:  Nat Genet       Date:  1995-05       Impact factor: 38.330
  2 in total
  2 in total

1.  Methylenetetrahydrofolate reductase C677T polymorphism and susceptibility to epilepsy.

Authors:  Vandana Rai; Pradeep Kumar
Journal:  Neurol Sci       Date:  2018-09-28       Impact factor: 3.307

2.  Association of Nicotinamide-N-Methyltransferase Gene rs694539 Variant with Epilepsy.

Authors:  Gensay Sazci; Bilgen Sazci; Ali Sazci; Halil Atilla Idrisoglu
Journal:  Mol Neurobiol       Date:  2015-07-28       Impact factor: 5.590
  2 in total

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