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dc.contributor.authorChan, LFen_US
dc.contributor.authorChung, TTen_US
dc.contributor.authorMassoud, AFen_US
dc.contributor.authorMetherell, LAen_US
dc.contributor.authorClark, AJLen_US
dc.date.accessioned2016-11-30T12:19:53Z
dc.date.issued2009-04en_US
dc.date.submitted2016-03-01T14:51:37.264Z
dc.identifier.issn0804-4643en_US
dc.identifier.other10.1530/EJE-08-0636
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/18034
dc.description.sponsorshipL F C and T-T C are supported by M R C Clinical Research Training Fellowships (grant numbers G0600408, G0700581) and L A M by the Wellcome Trust (grant number 076430/Z/05/7).en_US
dc.format.extent705 - 710en_US
dc.language.isoenen_US
dc.relation.ispartofEUR J ENDOCRINOLen_US
dc.rightsThis is an Open Access article distributed under the terms of the European Journal of Endocrinology's Re-use Licence which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
dc.subjectADRENOCORTICOTROPIN RECEPTOR GENEen_US
dc.subjectFAMILIAL GLUCOCORTICOID DEFICIENCYen_US
dc.subjectACTH RECEPTORen_US
dc.subjectSTEROIDOGENESISen_US
dc.subjectABNORMALITIESen_US
dc.subjectNEOPLASMSen_US
dc.subjectTUMORSen_US
dc.titleFunctional consequence of a novel Y129C mutation in a patient with two contradictory melanocortin-2-receptor mutationsen_US
dc.typeArticle
dc.rights.holder2009 European Society of Endocrinology
dc.identifier.doi10.1530/EJE-08-0636en_US
pubs.issue4en_US
pubs.notesNot knownen_US
pubs.volume160en_US


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