Heur, Martin <br/><br/>
Branch retinal artery occlusion associated with compound heterozygous genotype for methylenetetrahydrofolate reductase.  [electronic resource] 

 -  Documenta ophthalmologica. Advances in ophthalmology  May 2007 
 - 163-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S. 
<br/><br/><label>ISSN: </label>0012-4486 
<br/><br/><label>Standard No.: </label>10.1007/s10633-007-9051-3  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Electroretinography<br/>Female<br/>Genotype<br/>Homocysteine--blood<br/>Humans<br/>Hyperhomocysteinemia--genetics<br/>Methylenetetrahydrofolate Reductase (NADPH2)--genetics<br/>Polymorphism, Genetic<br/>Retinal Artery Occlusion--diagnosis<br/>Tomography, Optical Coherence<br/>Visual Field Tests<br/>Visual Fields