Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.
dc.contributor.author | Styrkarsdottir, Unnur | |
dc.contributor.author | Helgason, Hannes | |
dc.contributor.author | Sigurdsson, Asgeir | |
dc.contributor.author | Norddahl, Gudmundur L | |
dc.contributor.author | Agustsdottir, Arna B | |
dc.contributor.author | Reynard, Louise N | |
dc.contributor.author | Villalvilla, Amanda | |
dc.contributor.author | Halldorsson, Gisli H | |
dc.contributor.author | Jonasdottir, Aslaug | |
dc.contributor.author | Magnusdottir, Audur | |
dc.contributor.author | Oddson, Asmundur | |
dc.contributor.author | Sulem, Gerald | |
dc.contributor.author | Zink, Florian | |
dc.contributor.author | Sveinbjornsson, Gardar | |
dc.contributor.author | Helgason, Agnar | |
dc.contributor.author | Johannsdottir, Hrefna S | |
dc.contributor.author | Helgadottir, Anna | |
dc.contributor.author | Stefansson, Hreinn | |
dc.contributor.author | Gretarsdottir, Solveig | |
dc.contributor.author | Rafnar, Thorunn | |
dc.contributor.author | Almdahl, Ina S | |
dc.contributor.author | Brækhus, Anne | |
dc.contributor.author | Fladby, Tormod | |
dc.contributor.author | Selbæk, Geir | |
dc.contributor.author | Hosseinpanah, Farhad | |
dc.contributor.author | Azizi, Fereidoun | |
dc.contributor.author | Koh, Jung Min | |
dc.contributor.author | Tang, Nelson L S | |
dc.contributor.author | Danesphour, Maryams | |
dc.contributor.author | Mayordomo, Jose I | |
dc.contributor.author | Welt, Corrine | |
dc.contributor.author | Braund, Peter S | |
dc.contributor.author | Samani, Nilesh J | |
dc.contributor.author | Kiemeney, Lambertus A | |
dc.contributor.author | Lohmander, L Stefan | |
dc.contributor.author | Christiansen, Claus | |
dc.contributor.author | Andreassen, Ole A | |
dc.contributor.author | Consortium, arcOGEN | |
dc.contributor.author | Magnusson, Olafur | |
dc.contributor.author | Masson, Gisli | |
dc.contributor.author | Kong, Augustine | |
dc.contributor.author | Jonsdottir, Ingileif | |
dc.contributor.author | Gudbjartsson, Daniel | |
dc.contributor.author | Sulem, Patrick | |
dc.contributor.author | Jonsson, Helgi | |
dc.contributor.author | Loughlin, John | |
dc.contributor.author | Ingvarsson, Thorvaldur | |
dc.contributor.author | Thorsteinsdottir, Unnur | |
dc.contributor.author | Stefansson, Kari | |
dc.date.accessioned | 2018-03-05T15:32:44Z | |
dc.date.available | 2018-03-05T15:32:44Z | |
dc.date.issued | 2017 | |
dc.date.submitted | 2018 | |
dc.identifier.citation | Corrigendum: 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.issn | 1546-1718 | |
dc.identifier.pmid | 28747754 | |
dc.identifier.doi | 10.1038/ng0817-1286b | |
dc.identifier.uri | http://hdl.handle.net/2336/620494 | |
dc.description | To access publisher's full text version of this article click on the hyperlink below | en |
dc.language.iso | en | en |
dc.publisher | Nature Publishing Group | en |
dc.relation.url | https://www.nature.com/articles/ng0817-1286b.pdf | en |
dc.rights | Archived with thanks to Nature genetics | en |
dc.title | Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis. | en |
dc.type | Article | en |
dc.identifier.journal | Nature genetics | en |
dc.rights.access | Landspitali Access - LSH-aðgangur | en |