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

Internet

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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