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IL10 Low-Frequency Variants in Behçet's Disease Patients

dc.contributor.authorMatos, M
dc.contributor.authorXavier, JM
dc.contributor.authorAbrantes, P
dc.contributor.authorSousa, I
dc.contributor.authorRei, N
dc.contributor.authorDavatchi, F
dc.contributor.authorShahram, F
dc.contributor.authorJesus, G
dc.contributor.authorBarcelos, F
dc.contributor.authorVedes, J
dc.contributor.authorSalgado, Manuel
dc.contributor.authorAbdollahi, B
dc.contributor.authorNadji, A
dc.contributor.authorMoraes-Fontes, MF
dc.contributor.authorShafiee, N
dc.contributor.authorGhaderibarmi, F
dc.contributor.authorVaz Patto, J
dc.contributor.authorCrespo, J
dc.contributor.authorOliveira, SA
dc.date.accessioned2016-08-11T10:30:30Z
dc.date.available2016-08-11T10:30:30Z
dc.date.issued2014-04-08
dc.description.abstractTo explain the missing heritability after the genome-wide association studies era, sequencing studies allow the identification of low-frequency variants with a stronger effect on disease risk. Common variants in the interleukin 10 gene (IL10) have been consistently associated with Behçet's disease (BD) and the goal of this study is to investigate the role of low-frequency IL10 variants in BD susceptibility.pt_PT
dc.identifier.citationInt J Rheum Dis. 2014 Apr 8.pt_PT
dc.identifier.doi10.1111/1756-185X.12369pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/2548
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherWiley Publishingpt_PT
dc.subjectBehçet's diseasept_PT
dc.subjectIL10pt_PT
dc.subjectLow-frequency variantspt_PT
dc.subjectHCC DAUTOIMpt_PT
dc.titleIL10 Low-Frequency Variants in Behçet's Disease Patientspt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPagen/apt_PT
oaire.citation.startPagen/apt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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