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dc.contributor.authorO'Brien, NLen_US
dc.contributor.authorFiorentino, Aen_US
dc.contributor.authorCurtis, Den_US
dc.contributor.authorRayner, Cen_US
dc.contributor.authorPetrosellini, Cen_US
dc.contributor.authorAl Eissa, Men_US
dc.contributor.authorBass, NJen_US
dc.contributor.authorMcQuillin, Aen_US
dc.contributor.authorSharp, SIen_US
dc.date.accessioned2018-04-30T13:59:58Z
dc.date.available2018-03-01en_US
dc.date.issued2018-09en_US
dc.date.submitted2018-03-25T17:16:42.304Z
dc.identifier.issn0920-9964en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/36596
dc.description.sponsorshipUK Medical Research Council project grants G9623693N, G0500791, G0701007 and G1000708. NIHR University College London Hospitals Biomedical Research Centre (BRC) and UCLH Charitable Trustees/Clinical Research and Development Committee (CRDC).en_US
dc.format.extent181 - 188en_US
dc.language.isoenen_US
dc.relation.ispartofSCHIZOPHRENIA RESEARCHen_US
dc.subjectSequencingen_US
dc.subjectGenotypingen_US
dc.subjectPsychosisen_US
dc.subjectGenetic risken_US
dc.titleRare variant analysis in multiply affected families, association studies and functional analysis suggest a role for the ITGB4 gene in schizophrenia and bipolar disorderen_US
dc.typeArticle
dc.identifier.doi10.1016/j.schres.2018.03.001en_US
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000444845900028&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.notesNo embargoen_US
pubs.publication-statusPublisheden_US
pubs.volume199en_US


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