5,10-Methylenetetrahydrofolate reductase C677T gene polymorphism in Behcet's patients with or without ocular involvement.

Ozkul, Y; Evereklioglu, C; Borlu, M; Taheri, S; Calis, M; Dündar, M; Ilhan, O

Ozkul, Y; Evereklioglu, C; Borlu, M; Taheri, S; Calis, M; Dündar, M; Ilhan, O.

Affiliation

Ozkul Y; Sivas Cad Cebeci Apt A-Blok, 175/15, TR-38020, Kayseri, Turkey.

Br J Ophthalmol ; 89(12): 1634-7, 2005 Dec.

Article in En | MEDLINE | ID: mdl-16299146

Subject(s)

Behcet Syndrome/genetics; Methylenetetrahydrofolate Reductase (NADPH2)/genetics; Polymorphism, Genetic; Adult; Behcet Syndrome/blood; Female; Genetic Predisposition to Disease; Genotype; Homocysteine/blood; Humans; Male; Middle Aged; Panuveitis/genetics

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polymorphism, Genetic / Behcet Syndrome / Methylenetetrahydrofolate Reductase (NADPH2) Type of study: Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Br J Ophthalmol Year: 2005 Document type: Article Affiliation country: Turkey

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