Copy number variations and gene polymorphisms of Complement components in ocular Behcet’s disease and Vogt-Koyanagi-Harada syndrome

Complement is involved in many immune-mediated diseases. However, the association of its copy number variations (CNVs) and polymorphisms with Behcet’s disease (BD) and Vogt-Koyanagi-Harada syndrome (VKH) is unknown. We examined copy number and mRNA expression by real-time PCR. Cytokine production by...

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Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Sci Rep
Päätekijät: Xu, Dengfeng, Hou, Shengping, Zhang, Jun, Jiang, Yanni, Kijlstra, Aize, Yang, Peizeng
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Nature Publishing Group 2015
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4534762/
https://ncbi.nlm.nih.gov/pubmed/26269006
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep12989
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