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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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Detalles Bibliográficos
Autores principales:	Aslam, Muhammad Muaaz, John, Peter, Fan, Kang-Hsien, Bhatti, Attya, Feingold, Eleanor, Demirci, F. Yesim, Kamboh, M. Ilyas
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2020
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568136/ https://www.ncbi.nlm.nih.gov/pubmed/33101545 http://dx.doi.org/10.1155/2020/7189626

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