Cargando…
Clinical significance of NCOA5 gene rs2903908 polymorphism in Behçet's disease
Behçet's disease (BD) is an autoimmune multisystemic disease. The precise etiology of BD is not fully understood; however, it is thought that interactions between genetic and environmental factors play an essential role in its pathogenesis. The nuclear receptor coactivator-5 (NCOA5) gene encode...
Autores principales: | Rustemoglu, Aydin, Erkol Inal, Esra, Inanir, Ahmet, Ekinci, Duygu, Gul, Ulker, Yigit, Serbulent, Ates, Omer, Karakus, Nevin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Leibniz Research Centre for Working Environment and Human Factors
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491927/ https://www.ncbi.nlm.nih.gov/pubmed/28694762 http://dx.doi.org/10.17179/excli2017-189 |
Ejemplares similares
-
Association between the methylene tetrahydrofolate reductase gene C677T mutation and colchicine unresponsiveness in Behcet’s disease
por: Karakus, Nevin, et al.
Publicado: (2012) -
Association of MTHFR gene C677T mutation with diabetic peripheral neuropathy and diabetic retinopathy
por: Yigit, Serbulent, et al.
Publicado: (2013) -
Common Mediterranean Fever (MEFV) Gene Mutations Associated with Ankylosing Spondylitis in Turkish Population
por: Yigit, Serbulent, et al.
Publicado: (2012) -
Association of IL-4 gene VNTR variant with deep venous thrombosis in Behçet’s disease and its effect on ocular involvement
por: Inanir, Ahmet, et al.
Publicado: (2013) -
Investigation of Associations between Obesity and LEP G2548A and LEPR 668A/G Polymorphisms in a Turkish Population
por: Şahın, Server, et al.
Publicado: (2013)