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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388981/
https://www.ncbi.nlm.nih.gov/pubmed/22773907

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