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Sequencing PDX1 (insulin promoter factor 1) in 1788 UK individuals found 5% had a low frequency coding variant, but these variants are not associated with Type 2 diabetes

dc.contributor.authorEdghill, ELen_US
dc.contributor.authorKhamis, Aen_US
dc.contributor.authorWeedon, MNen_US
dc.contributor.authorWalker, Men_US
dc.contributor.authorHitman, GAen_US
dc.contributor.authorMcCarthy, MIen_US
dc.contributor.authorOwen, KRen_US
dc.contributor.authorEllard, Sen_US
dc.contributor.authorHattersley, ATen_US
dc.contributor.authorFrayling, TMen_US
dc.date.accessioned2016-08-30T08:43:07Z
dc.date.issued2011-06en_US
dc.date.submitted2016-08-03T17:42:09.832Z
dc.identifier.issn0742-3071en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/14892
dc.description.sponsorshipThis work was funded by the European Union (Integrated Project EURODIA LSHM-CT-2006-518153 in the Framework Programme 6 of the European Community). ATH and SE are employed as core members of the Peninsula NIHR Clinical Research Facility. KRO is an NIHR Clinician Scientist.en_US
dc.format.extent681 - 684en_US
dc.language.isoenen_US
dc.relation.ispartofDIABETIC MEDen_US
dc.subjectdiabetesen_US
dc.subjectgeneticsen_US
dc.subjectpolygenicen_US
dc.subjectvariantsen_US
dc.subjectFACTOR-Ien_US
dc.subjectD76N POLYMORPHISMen_US
dc.subjectGENEen_US
dc.subjectMUTATIONSen_US
dc.subjectSUSCEPTIBILITYen_US
dc.subjectPANCREASen_US
dc.subjectRISKen_US
dc.subjectIPF1en_US
dc.subjectPOPULATIONen_US
dc.subjectCONTRIBUTEen_US
dc.titleSequencing PDX1 (insulin promoter factor 1) in 1788 UK individuals found 5% had a low frequency coding variant, but these variants are not associated with Type 2 diabetesen_US
dc.typeArticle
dc.rights.holder(c) 2011 The Authors. Diabetic Medicine (c) 2011 Diabetes UK
dc.identifier.doi10.1111/j.1464-5491.2011.03269.xen_US
pubs.issue6en_US
pubs.notesNot knownen_US
pubs.volume28en_US


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