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Identification ofUBAP1mutations in juvenile hereditary spastic paraplegia in the 100,000 Genomes Project

dc.contributor.authorBourinaris, Ten_US
dc.contributor.authorSmedley, Den_US
dc.contributor.authorCipriani, Ven_US
dc.contributor.authorSheikh, Ien_US
dc.contributor.authorAthanasiou-Fragkouli, Aen_US
dc.contributor.authorChinnery, Pen_US
dc.contributor.authorMorris, Hen_US
dc.contributor.authorReal, Ren_US
dc.contributor.authorHarrison, Ven_US
dc.contributor.authorReid, Een_US
dc.contributor.authorWood, Nen_US
dc.contributor.authorVandrovcova, Jen_US
dc.contributor.authorHoulden, Hen_US
dc.contributor.authorTucci, Aen_US
dc.contributor.authorConsortium, GERen_US
dc.date.accessioned2020-09-16T17:09:50Z
dc.date.available2020-08-15en_US
dc.date.issued2020-09-15en_US
dc.identifier.issn1018-4813en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/67071
dc.language.isoenen_US
dc.relation.ispartofEUROPEAN JOURNAL OF HUMAN GENETICSen_US
dc.titleIdentification ofUBAP1mutations in juvenile hereditary spastic paraplegia in the 100,000 Genomes Projecten_US
dc.typeArticle
dc.identifier.doi10.1038/s41431-020-00720-wen_US
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000571167800001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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