Jaksic, Vesna <br/><br/>
MTHFR C677T homozygous mutation in a patient with pigmentary glaucoma and central retinal vein occlusion.  [electronic resource] 

 -  Ophthalmic research  2010 
 - 193-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1423-0259 
<br/><br/><label>Standard No.: </label>10.1159/000272023  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Antihypertensive Agents--therapeutic use<br/>Glaucoma, Open-Angle--blood<br/>Gonioscopy<br/>Homocysteine--blood<br/>Homozygote<br/>Humans<br/>Hyperhomocysteinemia--genetics<br/>Intraocular Pressure<br/>Male<br/>Methylenetetrahydrofolate Reductase (NADPH2)--genetics<br/>Mutation--genetics<br/>Polymorphism, Single Nucleotide--genetics<br/>Retinal Vein Occlusion--blood