MTHFR C677T Homozygous Mutation in a Patient with Pigmentary Glaucoma and Central Retinal Vein Occlusion | Citedby Results | Ophthalmic Research | Karger Publishers

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MTHFR C677T Homozygous Mutation in a Patient with Pigmentary Glaucoma and Central Retinal Vein Occlusion

Ophthalmic Res (2010) 43 (4): 193–196.

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