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dc.contributor.authorMeimaridou, Een_US
dc.contributor.authorKowalczyk, Jen_US
dc.contributor.authorGuasti, Len_US
dc.contributor.authorHughes, CRen_US
dc.contributor.authorWagner, Fen_US
dc.contributor.authorFrommolt, Pen_US
dc.contributor.authorNuernberg, Pen_US
dc.contributor.authorMann, NPen_US
dc.contributor.authorBanerjee, Ren_US
dc.contributor.authorSaka, HNen_US
dc.contributor.authorChapple, JPen_US
dc.contributor.authorKing, PJen_US
dc.contributor.authorClark, AJLen_US
dc.contributor.authorMetherell, LAen_US
dc.date.accessioned2016-11-30T12:58:51Z
dc.date.available2012-04-30en_US
dc.date.issued2012-07en_US
dc.date.submitted2016-03-01T14:55:49.791Z
dc.identifier.issn1061-4036en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/18037
dc.description.sponsorshipThis work has been supported by the Medical Research Council UK (New Investigator Research Grant G0801265 to L.A.M., Clinical Research Training Fellowship Grant G0901980 to C.R.H. and Project Grant G0700767 to P.J.K.).en_US
dc.format.extent740 - 742en_US
dc.language.isoenen_US
dc.relation.ispartofNATURE GENETICSen_US
dc.titleMutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiencyen_US
dc.typeArticle
dc.rights.holder2012. Nature America Inc.
dc.identifier.doi10.1038/ng.2299en_US
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000305886900005&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.issue7en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume44en_US


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