dc.contributor.author | Chan, LF | en_US |
dc.contributor.author | Chung, TT | en_US |
dc.contributor.author | Massoud, AF | en_US |
dc.contributor.author | Metherell, LA | en_US |
dc.contributor.author | Clark, AJL | en_US |
dc.date.accessioned | 2016-11-30T12:19:53Z | |
dc.date.issued | 2009-04 | en_US |
dc.date.submitted | 2016-03-01T14:51:37.264Z | |
dc.identifier.issn | 0804-4643 | en_US |
dc.identifier.other | 10.1530/EJE-08-0636 | |
dc.identifier.uri | http://qmro.qmul.ac.uk/xmlui/handle/123456789/18034 | |
dc.description.sponsorship | L 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.extent | 705 - 710 | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | EUR J ENDOCRINOL | en_US |
dc.rights | This 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.subject | ADRENOCORTICOTROPIN RECEPTOR GENE | en_US |
dc.subject | FAMILIAL GLUCOCORTICOID DEFICIENCY | en_US |
dc.subject | ACTH RECEPTOR | en_US |
dc.subject | STEROIDOGENESIS | en_US |
dc.subject | ABNORMALITIES | en_US |
dc.subject | NEOPLASMS | en_US |
dc.subject | TUMORS | en_US |
dc.title | Functional consequence of a novel Y129C mutation in a patient with two contradictory melanocortin-2-receptor mutations | en_US |
dc.type | Article | |
dc.rights.holder | 2009 European Society of Endocrinology | |
dc.identifier.doi | 10.1530/EJE-08-0636 | en_US |
pubs.issue | 4 | en_US |
pubs.notes | Not known | en_US |
pubs.volume | 160 | en_US |