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Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency

dc.contributor.authorChan, LFen_US
dc.contributor.authorMetherell, LAen_US
dc.contributor.authorKrude, Hen_US
dc.contributor.authorBall, Cen_US
dc.contributor.authorO'Riordan, SMPen_US
dc.contributor.authorCostigan, Cen_US
dc.contributor.authorLynch, SAen_US
dc.contributor.authorSavage, MOen_US
dc.contributor.authorCavarzere, Pen_US
dc.contributor.authorClark, AJLen_US
dc.date.accessioned2016-11-30T13:32:07Z
dc.date.issued2009-08en_US
dc.date.submitted2016-03-01T14:56:31.631Z
dc.identifier.issn0300-0664en_US
dc.identifier.other10.1111/j.1365-2265.2008.03511.x
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/18040
dc.description.sponsorshipLFC is a MRC Clinical Research Training Fellow and LAM is supported by the Wellcome Trust.en_US
dc.format.extent171 - 175en_US
dc.language.isoenen_US
dc.relation.ispartofCLIN ENDOCRINOLen_US
dc.rightsCreative Commons Deed, Attribution 2·5, which does not permit commercial exploitation.
dc.subjectMELANOCORTIN 2 RECEPTORen_US
dc.subjectADRENOCORTICOTROPIN RECEPTORen_US
dc.subjectFUNCTIONAL-CHARACTERIZATIONen_US
dc.subjectGENEen_US
dc.subjectABNORMALITIESen_US
dc.subjectMICEen_US
dc.titleHomozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiencyen_US
dc.typeArticle
dc.rights.holder2009. The authors
dc.identifier.doi10.1111/j.1365-2265.2008.03511.xen_US
pubs.issue2en_US
pubs.notesNot knownen_US
pubs.volume71en_US


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