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A whole genome screen for association with multiple sclerosis in Portuguese patients

2003Journal article Open access
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dc.contributor.authorSantos, M
dc.contributor.authorPinto-Basto, J
dc.contributor.authorRio, ME
dc.contributor.authorSá, MJ
dc.contributor.authorValença, A
dc.contributor.authorSá, A
dc.contributor.authorDinis, J
dc.contributor.authorFigueiredo, J
dc.contributor.authorBigotte de Almeida, L
dc.contributor.authorCoelho, I
dc.contributor.authorSawcer, S
dc.contributor.authorSetakis, E
dc.contributor.authorCompston, A
dc.contributor.authorSequeiros, J
dc.contributor.authorMaciel, P
dc.date.accessioned2013-11-11T18:53:52Z
dc.date.available2013-11-11T18:53:52Z
dc.date.issued2003
dc.description.abstractMultiple sclerosis (MS) is common in Europe affecting up to 1:500 people. In an effort to identify genes influencing susceptibility to the disease, we have performed a population-based whole genome screen for association. In this study, 6000 microsatellite markers were typed in separately pooled DNA samples from MS patients (n=188) and matched controls (n=188). Interpretable data was obtained from 4661 of these markers. Refining analysis of the most promising markers identified 10 showing potential evidence for association.por
dc.identifier.citationJ Neuroimmunol. 2003;143(1-2):112-5.por
dc.identifier.urihttp://hdl.handle.net/10400.26/4876
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherElsevierpor
dc.subjectPredisposição Genética para Doençapor
dc.subjectPortugalpor
dc.subjectEsclerose Múltiplapor
dc.subjectTestes Genéticospor
dc.titleA whole genome screen for association with multiple sclerosis in Portuguese patientspor
dc.typejournal article
dspace.entity.typePublication
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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