%0 Journal Article
%T Investigation of methylenetetrahydrofolate reductase C677T and factor V Leiden mutation as a genetic marker for retinal vein occlusion
%A Nitin Nema
%A Ravindra Kumar
%A Sonam Verma
%J Archive of "Taiwan Journal of Ophthalmology".
%D 2018
%R 10.4103/tjo.tjo_43_17
%X Thromboembolic phenomenon is one of the causes of retinal vein occlusion (RVO) which is in fact a multifactorial disease. Therefore, we aimed to study methylenetetrahydrofolate reductase gene polymorphism (MTHFR C677T) and factor V Leiden as genetic risk factors of RVO
%K Factor V Leiden
%K hyperhomocysteinemia
%K methylenetetrahydrofolate reductase
%K retinal vein occlusion
%U https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6055313/