Association between the methylene tetrahydrofolate reductase gene C677T mutation and colchicine unresponsiveness in Behcet’s disease

PURPOSE: Behcet’s disease (BD) is a multisystemic immunoinflammatory disorder characterized by mucocutaneous, ocular, vascular, and central nervous system manifestations. The common methylene tetrahydrofolate reductase (MTHFR) gene C677T mutation is a known risk factor for thrombosis. The aim of thi...

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Autores principales: Karakus, Nevin, Yigit, Serbulent, Kalkan, Goknur, Rustemoglu, Aydin, Inanir, Ahmet, Gul, Ulker, Pancar, Gunseli Sefika, Akkanet, Songul, Ates, Omer
Formato: Artigo
Lenguaje:Inglês
Publicado: Molecular Vision 2012
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Research Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3388981/
https://ncbi.nlm.nih.gov/pubmed/22773907
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