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dc.contributor.authorBarøy, Tuva
dc.contributor.authorMisceo, Doriana
dc.contributor.authorStrømme, Petter
dc.contributor.authorStray-Pedersen, Asbjørg
dc.contributor.authorHolmgren, Asbjørn
dc.contributor.authorRødningen, Olaug K
dc.contributor.authorBlomhoff, Anne
dc.contributor.authorHelle, Johan R
dc.contributor.authorStormyr, Alice
dc.contributor.authorTvedt, Bjørn
dc.contributor.authorFannemel, Madeleine
dc.contributor.authorFrengen, Eirik
dc.date.accessioned2015-10-20T10:52:30Z
dc.date.available2015-10-20T10:52:30Z
dc.date.issued2013
dc.identifier.citationOrphanet Journal of Rare Diseases. 2013 Jan 07;8(1):3
dc.identifier.urihttp://hdl.handle.net/10852/46993
dc.language.isoeng
dc.rightsBarøy et al; licensee BioMed Central Ltd.
dc.rightsAttribution 2.0 Generic
dc.rights.urihttp://creativecommons.org/licenses/by/2.0/
dc.titleHaploinsufficiency of two histone modifier genes on 6p22.3, ATXN1 and JARID2, is associated with intellectual disability
dc.typeJournal article
dc.date.updated2015-10-20T10:52:31Z
dc.creator.authorBarøy, Tuva
dc.creator.authorMisceo, Doriana
dc.creator.authorStrømme, Petter
dc.creator.authorStray-Pedersen, Asbjørg
dc.creator.authorHolmgren, Asbjørn
dc.creator.authorRødningen, Olaug K
dc.creator.authorBlomhoff, Anne
dc.creator.authorHelle, Johan R
dc.creator.authorStormyr, Alice
dc.creator.authorTvedt, Bjørn
dc.creator.authorFannemel, Madeleine
dc.creator.authorFrengen, Eirik
dc.identifier.doihttp://dx.doi.org/10.1186/1750-1172-8-3
dc.identifier.urnURN:NBN:no-51150
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/46993/1/13023_2012_Article_553.pdf
dc.type.versionPublishedVersion
cristin.articleid3


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