Investigation of methylenetetrahydrofolate reductase C677T and factor V Leiden mutation as a genetic marker for retinal vein occlusion

PURPOSE: 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. MATERIALS AND METHOD...

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Detalles Bibliográficos
Autores principales: Nema, Nitin, Verma, Sonam, Kumar, Ravindra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6055313/
https://www.ncbi.nlm.nih.gov/pubmed/30038889
http://dx.doi.org/10.4103/tjo.tjo_43_17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6055313/
https://www.ncbi.nlm.nih.gov/pubmed/30038889
http://dx.doi.org/10.4103/tjo.tjo_43_17

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