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Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.

dc.contributor.authorStyrkarsdottir, Unnur
dc.contributor.authorHelgason, Hannes
dc.contributor.authorSigurdsson, Asgeir
dc.contributor.authorNorddahl, Gudmundur L
dc.contributor.authorAgustsdottir, Arna B
dc.contributor.authorReynard, Louise N
dc.contributor.authorVillalvilla, Amanda
dc.contributor.authorHalldorsson, Gisli H
dc.contributor.authorJonasdottir, Aslaug
dc.contributor.authorMagnusdottir, Audur
dc.contributor.authorOddson, Asmundur
dc.contributor.authorSulem, Gerald
dc.contributor.authorZink, Florian
dc.contributor.authorSveinbjornsson, Gardar
dc.contributor.authorHelgason, Agnar
dc.contributor.authorJohannsdottir, Hrefna S
dc.contributor.authorHelgadottir, Anna
dc.contributor.authorStefansson, Hreinn
dc.contributor.authorGretarsdottir, Solveig
dc.contributor.authorRafnar, Thorunn
dc.contributor.authorAlmdahl, Ina S
dc.contributor.authorBrækhus, Anne
dc.contributor.authorFladby, Tormod
dc.contributor.authorSelbæk, Geir
dc.contributor.authorHosseinpanah, Farhad
dc.contributor.authorAzizi, Fereidoun
dc.contributor.authorKoh, Jung Min
dc.contributor.authorTang, Nelson L S
dc.contributor.authorDanesphour, Maryams
dc.contributor.authorMayordomo, Jose I
dc.contributor.authorWelt, Corrine
dc.contributor.authorBraund, Peter S
dc.contributor.authorSamani, Nilesh J
dc.contributor.authorKiemeney, Lambertus A
dc.contributor.authorLohmander, L Stefan
dc.contributor.authorChristiansen, Claus
dc.contributor.authorAndreassen, Ole A
dc.contributor.authorConsortium, arcOGEN
dc.contributor.authorMagnusson, Olafur
dc.contributor.authorMasson, Gisli
dc.contributor.authorKong, Augustine
dc.contributor.authorJonsdottir, Ingileif
dc.contributor.authorGudbjartsson, Daniel
dc.contributor.authorSulem, Patrick
dc.contributor.authorJonsson, Helgi
dc.contributor.authorLoughlin, John
dc.contributor.authorIngvarsson, Thorvaldur
dc.contributor.authorThorsteinsdottir, Unnur
dc.contributor.authorStefansson, Kari
dc.date.accessioned2018-03-05T15:32:44Z
dc.date.available2018-03-05T15:32:44Z
dc.date.issued2017
dc.date.submitted2018
dc.identifier.citationCorrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis. 2017, 49 (8):1286 Nat. Genet.en
dc.identifier.issn1546-1718
dc.identifier.pmid28747754
dc.identifier.doi10.1038/ng0817-1286b
dc.identifier.urihttp://hdl.handle.net/2336/620494
dc.descriptionTo access publisher's full text version of this article click on the hyperlink belowen
dc.language.isoenen
dc.publisherNature Publishing Groupen
dc.relation.urlhttps://www.nature.com/articles/ng0817-1286b.pdfen
dc.rightsArchived with thanks to Nature geneticsen
dc.titleCorrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.en
dc.typeArticleen
dc.identifier.journalNature geneticsen
dc.rights.accessLandspitali Access - LSH-aðganguren


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