dc.contributor.author | Meimaridou, E | en_US |
dc.contributor.author | Kowalczyk, J | en_US |
dc.contributor.author | Guasti, L | en_US |
dc.contributor.author | Hughes, CR | en_US |
dc.contributor.author | Wagner, F | en_US |
dc.contributor.author | Frommolt, P | en_US |
dc.contributor.author | Nuernberg, P | en_US |
dc.contributor.author | Mann, NP | en_US |
dc.contributor.author | Banerjee, R | en_US |
dc.contributor.author | Saka, HN | en_US |
dc.contributor.author | Chapple, JP | en_US |
dc.contributor.author | King, PJ | en_US |
dc.contributor.author | Clark, AJL | en_US |
dc.contributor.author | Metherell, LA | en_US |
dc.date.accessioned | 2016-11-30T12:58:51Z | |
dc.date.available | 2012-04-30 | en_US |
dc.date.issued | 2012-07 | en_US |
dc.date.submitted | 2016-03-01T14:55:49.791Z | |
dc.identifier.issn | 1061-4036 | en_US |
dc.identifier.uri | http://qmro.qmul.ac.uk/xmlui/handle/123456789/18037 | |
dc.description.sponsorship | This 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.extent | 740 - 742 | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | NATURE GENETICS | en_US |
dc.title | Mutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiency | en_US |
dc.type | Article | |
dc.rights.holder | 2012. Nature America Inc. | |
dc.identifier.doi | 10.1038/ng.2299 | en_US |
pubs.author-url | http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000305886900005&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6a | en_US |
pubs.issue | 7 | en_US |
pubs.notes | Not known | en_US |
pubs.publication-status | Published | en_US |
pubs.volume | 44 | en_US |