Association of copy number variation in the FCGR3B gene with risk of autoimmune diseases

dc.creatorMamtani, M
dc.creatorAnaya, Juan-Manuel
dc.creatorHe, W
dc.creatorAhuja, S K
dc.date.accessioned2020-08-06T16:20:37Z
dc.date.accessioned2022-09-22T14:40:45Z
dc.date.available2020-08-06T16:20:37Z
dc.date.available2022-09-22T14:40:45Z
dc.date.created2020-08-06T16:20:37Z
dc.identifierISSN: 1476-5470
dc.identifierhttps://repository.urosario.edu.co/handle/10336/26080
dc.identifierhttps://doi.org/10.1038/gene.2009.71
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3441153
dc.description.abstractCopy number variation (CNV) of human DNA segments is an important source of genetic diversity and increasing evidence indicates that CNV may underlie disease susceptibility.1–4 It is to be noted that there seems to be an enrichment of CNV in immune response genes1 such that they may contribute to the observed inter-individual variability in susceptibility to infectious diseases, vasculitis and autoimmune diseases
dc.languageeng
dc.publisherMacmillan Publishers Limited
dc.relationGenes & Immunity, ISSN: 1476-5470,Vol.11, No.2 (2010-03); pp.155-160
dc.relationhttps://www.nature.com/articles/gene200971.pdf
dc.relation160
dc.relationNo. 2
dc.relation155
dc.relationGenes & Immunity
dc.relationVol. 11
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightsAbierto (Texto Completo)
dc.sourceGenes & Immunity
dc.sourceinstname:Universidad del Rosario
dc.sourcereponame:Repositorio Institucional EdocUR
dc.subjectGenoma Humano
dc.subjectFCGR3B
dc.subjectGenes de respuesta inmune
dc.titleAssociation of copy number variation in the FCGR3B gene with risk of autoimmune diseases
dc.typearticle


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