Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.
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Authors
Styrkarsdottir, UnnurHelgason, Hannes
Sigurdsson, Asgeir
Norddahl, Gudmundur L
Agustsdottir, Arna B
Reynard, Louise N
Villalvilla, Amanda
Halldorsson, Gisli H
Jonasdottir, Aslaug
Magnusdottir, Audur
Oddson, Asmundur
Sulem, Gerald
Zink, Florian
Sveinbjornsson, Gardar
Helgason, Agnar
Johannsdottir, Hrefna S
Helgadottir, Anna
Stefansson, Hreinn
Gretarsdottir, Solveig
Rafnar, Thorunn
Almdahl, Ina S
Brækhus, Anne
Fladby, Tormod
Selbæk, Geir
Hosseinpanah, Farhad
Azizi, Fereidoun
Koh, Jung Min
Tang, Nelson L S
Danesphour, Maryams
Mayordomo, Jose I
Welt, Corrine
Braund, Peter S
Samani, Nilesh J
Kiemeney, Lambertus A
Lohmander, L Stefan
Christiansen, Claus
Andreassen, Ole A
Consortium, arcOGEN
Magnusson, Olafur
Masson, Gisli
Kong, Augustine
Jonsdottir, Ingileif
Gudbjartsson, Daniel
Sulem, Patrick
Jonsson, Helgi
Loughlin, John
Ingvarsson, Thorvaldur
Thorsteinsdottir, Unnur
Stefansson, Kari
Issue Date
2017
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Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis. 2017, 49 (8):1286 Nat. Genet.Description
To access publisher's full text version of this article click on the hyperlink belowAdditional Links
https://www.nature.com/articles/ng0817-1286b.pdfRights
Archived with thanks to Nature geneticsae974a485f413a2113503eed53cd6c53
10.1038/ng0817-1286b
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