MTHFR C677T homozygous mutation in a patient with pigmentary glaucoma and central retinal vein occlusion.

Ophthalmic research

Volumn 43, Issue 4, 2010, Pages 193-196

  Jaksic, Vesna ^a   Markovic, Vujica ^b   Milenkovic, Svetislav ^b   Stefanovic, Ivan ^b   Jakovic, Natalija ^b   Knezevic, Miroslav ^b  

^a UNIVERSITY OF BELGRADE   (Serbia)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ANTIHYPERTENSIVE AGENT; HOMOCYSTEINE; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2);

ADULT; ARTICLE; BLOOD; CASE REPORT; GENETICS; GONIOSCOPY; HOMOZYGOTE; HUMAN; HYPERHOMOCYSTEINEMIA; INTRAOCULAR PRESSURE; MALE; MUTATION; OPEN ANGLE GLAUCOMA; RETINA VEIN OCCLUSION; SINGLE NUCLEOTIDE POLYMORPHISM;

ADULT; ANTIHYPERTENSIVE AGENTS; GLAUCOMA, OPEN-ANGLE; GONIOSCOPY; HOMOCYSTEINE; HOMOZYGOTE; HUMANS; HYPERHOMOCYSTEINEMIA; INTRAOCULAR PRESSURE; MALE; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; RETINAL VEIN OCCLUSION;

EID: 73649148756     PISSN: None     EISSN: 14230259     Source Type: Journal    
DOI: 10.1159/000272023     Document Type: Article

References (0)