Association of VPREB1 Gene Copy Number Variation and Rheumatoid Arthritis Susceptibility

OBJECTIVE: Copy number variation (CNV) is a structural variation in the human genome that has been associated with multiple clinical phenotypes. B cells are important components of rheumatoid arthritis- (RA-) mediated immune response; hence, CNV in the regulators of B cells (such as VPREB1) can infl...

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Detalhes bibliográficos
Publicado no:Dis Markers
Main Authors: Aslam, Muhammad Muaaz, John, Peter, Fan, Kang-Hsien, Bhatti, Attya, Feingold, Eleanor, Demirci, F. Yesim, Kamboh, M. Ilyas
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi 2020
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7568136/
https://ncbi.nlm.nih.gov/pubmed/33101545
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/7189626
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