dc.contributor.author | Barøy, Tuva | |
dc.contributor.author | Misceo, Doriana | |
dc.contributor.author | Strømme, Petter | |
dc.contributor.author | Stray-Pedersen, Asbjørg | |
dc.contributor.author | Holmgren, Asbjørn | |
dc.contributor.author | Rødningen, Olaug K | |
dc.contributor.author | Blomhoff, Anne | |
dc.contributor.author | Helle, Johan R | |
dc.contributor.author | Stormyr, Alice | |
dc.contributor.author | Tvedt, Bjørn | |
dc.contributor.author | Fannemel, Madeleine | |
dc.contributor.author | Frengen, Eirik | |
dc.date.accessioned | 2015-10-20T10:52:30Z | |
dc.date.available | 2015-10-20T10:52:30Z | |
dc.date.issued | 2013 | |
dc.identifier.citation | Orphanet Journal of Rare Diseases. 2013 Jan 07;8(1):3 | |
dc.identifier.uri | http://hdl.handle.net/10852/46993 | |
dc.language.iso | eng | |
dc.rights | Barøy et al; licensee BioMed Central Ltd. | |
dc.rights | Attribution 2.0 Generic | |
dc.rights.uri | http://creativecommons.org/licenses/by/2.0/ | |
dc.title | Haploinsufficiency of two histone modifier genes on 6p22.3, ATXN1 and JARID2, is associated with intellectual disability | |
dc.type | Journal article | |
dc.date.updated | 2015-10-20T10:52:31Z | |
dc.creator.author | Barøy, Tuva | |
dc.creator.author | Misceo, Doriana | |
dc.creator.author | Strømme, Petter | |
dc.creator.author | Stray-Pedersen, Asbjørg | |
dc.creator.author | Holmgren, Asbjørn | |
dc.creator.author | Rødningen, Olaug K | |
dc.creator.author | Blomhoff, Anne | |
dc.creator.author | Helle, Johan R | |
dc.creator.author | Stormyr, Alice | |
dc.creator.author | Tvedt, Bjørn | |
dc.creator.author | Fannemel, Madeleine | |
dc.creator.author | Frengen, Eirik | |
dc.identifier.doi | http://dx.doi.org/10.1186/1750-1172-8-3 | |
dc.identifier.urn | URN:NBN:no-51150 | |
dc.type.document | Tidsskriftartikkel | |
dc.type.peerreviewed | Peer reviewed | |
dc.identifier.fulltext | Fulltext https://www.duo.uio.no/bitstream/handle/10852/46993/1/13023_2012_Article_553.pdf | |
dc.type.version | PublishedVersion | |
cristin.articleid | 3 | |