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dc.contributor.authorHolliday, Kate L.
dc.contributor.authorThomson, Wendy
dc.contributor.authorNeogi, Tuhina
dc.contributor.authorFelson, David T.
dc.contributor.authorWang, Ke
dc.contributor.authorWu, Frederick C.
dc.contributor.authorHuhtaniemi, Ilpo T.
dc.contributor.authorBartfai, Gyorgy
dc.contributor.authorCasanueva, Felipe
dc.contributor.authorForti, Gianni
dc.contributor.authorKula, Krzysztof
dc.contributor.authorPunab, Margus
dc.contributor.authorVanderschueren, Dirk
dc.contributor.authorMacfarlane, Gary J.
dc.contributor.authorHoran, Michael A.
dc.contributor.authorOllier, William
dc.contributor.authorPayton, Antony
dc.contributor.authorPendleton, Neil
dc.contributor.authorMcBeth, John
dc.date.accessioned2019-05-13T13:30:11Z
dc.date.available2019-05-13T13:30:11Z
dc.date.issued2012-09-24
dc.identifier.citationHolliday , K L , Thomson , W , Neogi , T , Felson , D T , Wang , K , Wu , F C , Huhtaniemi , I T , Bartfai , G , Casanueva , F , Forti , G , Kula , K , Punab , M , Vanderschueren , D , Macfarlane , G J , Horan , M A , Ollier , W , Payton , A , Pendleton , N & McBeth , J 2012 , ' The non-synonymous SNP, R1150W, in SCN9A is not associated with chronic widespread pain susceptibility ' Molecular Pain , vol. 8 , 72 . https://doi.org/10.1186/1744-8069-8-72en
dc.identifier.issn1744-8069
dc.identifier.otherPURE: 139786107
dc.identifier.otherPURE UUID: 7009181c-e0f9-4025-8376-1d35372df658
dc.identifier.otherScopus: 84866502256
dc.identifier.otherPubMed: 23006801
dc.identifier.urihttp://hdl.handle.net/2164/12260
dc.identifier.urihttp://www.scopus.com/inward/record.url?scp=84866502256&partnerID=8YFLogxKen
dc.descriptionAcknowledgements The authors wish to thank all of the primary care practices and participants in the EPIFUND study, the EPIFUND study team and Arthritis Research UK lab staff for carrying out the genotyping. The authors thank the men who participated in the seven countries and the research/nursing staff in the seven centres of the EMAS study used in the current analysis: C Pott (Manchester), E Wouters (Leuven), M del Mar Fernandez (Santiago de Compostela), M Jedrzejowska (Lodz), H-M Tabo (Tartu) and A Heredi (Szeged) for their data collection, and C Moseley (Manchester) for data entry and project coordination. DV and SB are senior clinical investigators of the Fund for Scientific Research-Flanders, Belgium (F W O-Vlaanderen). SB is holder of the Leuven University Chair in Gerontology and Geriatrics. The researchers thank the Framingham study participants and personnel. This work was supported by Arthritis Research UK, Chesterfield, UK. The European Male Ageing Study (EMAS) is funded by the Commission of the European Communities Fifth Framework Programme ‘Quality of life and management of living resources’ grant QLK6-CT-2001-00258. Genotyping of the Dyne Steel DNA Bank for Ageing and Cognition cohort was supported by the BBSRC and the study was supported by AgeUK. The Framingham study was supported by grants from the National Heart, Lung, and Blood Institute (NHLBI contract N01-HC-25195) and NIH AR47785 and AG18393.en
dc.format.extent5en
dc.language.isoeng
dc.relation.ispartofMolecular Painen
dc.rights© 2012 Holliday et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en
dc.subjectChronic widespread painen
dc.subjectPopulation-based cohortsen
dc.subjectSingle nucleotide polymorphismen
dc.subjectVoltage-gated sodium channelen
dc.subjectR Medicine (General)en
dc.subjectMolecular Medicineen
dc.subjectCellular and Molecular Neuroscienceen
dc.subjectAnesthesiology and Pain Medicineen
dc.subject.lccR1en
dc.titleThe non-synonymous SNP, R1150W, in SCN9A is not associated with chronic widespread pain susceptibilityen
dc.typeJournal articleen
dc.contributor.institutionUniversity of Aberdeen, Other Applied Health Sciencesen
dc.contributor.institutionUniversity of Aberdeen, Epidemiology Groupen
dc.contributor.institutionUniversity of Aberdeen, Institute of Applied Health Sciencesen
dc.description.statusPeer revieweden
dc.description.versionPublisher PDFen
dc.identifier.doihttps://doi.org/10.1186/1744-8069-8-72


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