MTHFR C677T homozygous mutation in a patient with pigmentary glaucoma and central retinal vein occlusion. [electronic resource]
Producer: 20100621Description: 193-6 p. digitalISSN:- 1423-0259
- Adult
- Antihypertensive Agents -- therapeutic use
- Glaucoma, Open-Angle -- blood
- Gonioscopy
- Homocysteine -- blood
- Homozygote
- Humans
- Hyperhomocysteinemia -- genetics
- Intraocular Pressure
- Male
- Methylenetetrahydrofolate Reductase (NADPH2) -- genetics
- Mutation -- genetics
- Polymorphism, Single Nucleotide -- genetics
- Retinal Vein Occlusion -- blood
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Publication Type: Case Reports; Journal Article
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