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Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study

dc.contributor.authorMead, S.
dc.contributor.authorPoulter, M.
dc.contributor.authorUphill, J.
dc.contributor.authorBeck, J.
dc.contributor.authorWhitfield, Jerome
dc.contributor.authorWebb, T.
dc.contributor.authorCampbell, T.
dc.contributor.authorAdamson, G.
dc.contributor.authorDeriziotis, P.
dc.contributor.authorTabrizi, S.
dc.contributor.authorHummerich, H.
dc.contributor.authorVerzilli, C.
dc.contributor.authorAlpers, Michael Philip
dc.contributor.authorWhittaker, J.
dc.contributor.authorCollinge, J.
dc.date.accessioned2017-01-30T15:15:50Z
dc.date.available2017-01-30T15:15:50Z
dc.date.created2015-03-03T20:14:18Z
dc.date.issued2009
dc.identifier.citationMead, S. and Poulter, M. and Uphill, J. and Beck, J. and Whitfield, J. and Webb, T. and Campbell, T. et al. 2009. Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study. The Lancet Neurology. 8 (1): pp. 57-66.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/44701
dc.identifier.doi10.1016/S1474-4422(08)70265-5
dc.publisherThe Lancet Publishing Group
dc.titleGenetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study
dc.typeJournal Article
dcterms.source.volume8
dcterms.source.number1
dcterms.source.startPage57
dcterms.source.endPage66
dcterms.source.issn1474-4422
dcterms.source.titleThe Lancet Neurology
curtin.accessStatusOpen access via publisher


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