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

La variación del número de copias (CNV) en el genoma humano es un determinante importante de la susceptibilidad a las enfermedades autoinmunes. Muchas enfermedades autoinmunes comparten características clínicas y patógenas similares. Por lo tanto, las CNV de genes implicados en la inmunidad pueden s...

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Fecha de publicación:: 2010

Institución:: Universidad del Rosario

Repositorio:: Repositorio EdocUR - U. Rosario

Idioma:: eng

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dc.title.spa.fl_str_mv	Association of copy number variation in the FCGR3B gene with risk of autoimmune diseases
dc.title.TranslatedTitle.spa.fl_str_mv	Asociación de la variación del número de copias en el gen FCGR3B con riesgo de enfermedades autoinmunes
title	Association of copy number variation in the FCGR3B gene with risk of autoimmune diseases
spellingShingle	Association of copy number variation in the FCGR3B gene with risk of autoimmune diseases Genoma Humano FCGR3B Genes de respuesta inmune copy number variation (CNV) FCGR3B systemic lupus erythematosus Sjo¨gren’s syndrome CCL3L1
title_short	Association of copy number variation in the FCGR3B gene with risk of autoimmune diseases
title_full	Association of copy number variation in the FCGR3B gene with risk of autoimmune diseases
title_fullStr	Association of copy number variation in the FCGR3B gene with risk of autoimmune diseases
title_full_unstemmed	Association of copy number variation in the FCGR3B gene with risk of autoimmune diseases
title_sort	Association of copy number variation in the FCGR3B gene with risk of autoimmune diseases
dc.subject.spa.fl_str_mv	Genoma Humano FCGR3B Genes de respuesta inmune
topic	Genoma Humano FCGR3B Genes de respuesta inmune copy number variation (CNV) FCGR3B systemic lupus erythematosus Sjo¨gren’s syndrome CCL3L1
dc.subject.keyword.spa.fl_str_mv	copy number variation (CNV) FCGR3B systemic lupus erythematosus Sjo¨gren’s syndrome
dc.subject.keyword.eng.fl_str_mv	CCL3L1
description	La variación del número de copias (CNV) en el genoma humano es un determinante importante de la susceptibilidad a las enfermedades autoinmunes. Muchas enfermedades autoinmunes comparten características clínicas y patógenas similares. Por lo tanto, las CNV de genes implicados en la inmunidad pueden servir como determinantes compartidos de múltiples enfermedades autoinmunes.
publishDate	2010
dc.date.created.spa.fl_str_mv	2010-03
dc.date.accessioned.none.fl_str_mv	2020-08-06T16:20:37Z
dc.date.available.none.fl_str_mv	2020-08-06T16:20:37Z
dc.type.eng.fl_str_mv	article
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dc.type.spa.spa.fl_str_mv	Artículo
dc.identifier.doi.none.fl_str_mv	https://doi.org/10.1038/gene.2009.71
dc.identifier.issn.none.fl_str_mv	ISSN: 1476-5470
dc.identifier.uri.none.fl_str_mv	https://repository.urosario.edu.co/handle/10336/26080
url	https://doi.org/10.1038/gene.2009.71 https://repository.urosario.edu.co/handle/10336/26080
identifier_str_mv	ISSN: 1476-5470
dc.language.iso.spa.fl_str_mv	eng
language	eng
dc.relation.citationEndPage.none.fl_str_mv	160
dc.relation.citationIssue.none.fl_str_mv	No. 2
dc.relation.citationStartPage.none.fl_str_mv	155
dc.relation.citationTitle.none.fl_str_mv	Genes & Immunity
dc.relation.citationVolume.none.fl_str_mv	Vol. 11
dc.relation.ispartof.spa.fl_str_mv	Genes & Immunity, ISSN: 1476-5470,Vol.11, No.2 (2010-03); pp.155-160
dc.relation.uri.spa.fl_str_mv	https://www.nature.com/articles/gene200971.pdf
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dc.source.spa.fl_str_mv	Genes & Immunity
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Association of copy number variation in the FCGR3B gene with risk of autoimmune diseases

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