MTHFR C677T homozygous mutation in a patient with pigmentary glaucoma and central retinal vein occlusion. (Q43196100)
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scientific article published on 31 December 2009
Language | Label | Description | Also known as |
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English | MTHFR C677T homozygous mutation in a patient with pigmentary glaucoma and central retinal vein occlusion. |
scientific article published on 31 December 2009 |
Statements
MTHFR C677T homozygous mutation in a patient with pigmentary glaucoma and central retinal vein occlusion (English)
Vujica Markovic
Svetislav Milenkovic
Ivan Stefanovic
Natalija Jakovic
Miroslav Knezevic
31 December 2009