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Article

Hyperhomocysteinemia and the methylenetetrahydrofolate reductase 677C-T mutation in patients under 50 years of age affected by central retinal vein occlusion

1 May 2004

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 15121372
DOI: 10.1016/j.ophtha.2003.08.028

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Hyperhomocysteinemia and the methylenetetrahydrofolate reductase 677C-T mutation in patients under 50 years of age affected by central retinal vein occlusionPMID 15121372Read ↗

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A common mutation in the methylenetetrahydrofolate reductase gene is a determinant of hyperhomocysteinemia in epileptic patients receiving anticonvulsantsSemantic proximity Read ↗

Methylenetetrahydrofolatereductase (MTHFR) 677C>T polymorphism and open angle glaucoma.Semantic proximity Read ↗

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