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GHR transcript heterogeneity may explain the phenotypic variability in patients with homozygous GHR pseudoexon (6 Psi) mutation

dc.contributor.authorChatterjee, Sen_US
dc.contributor.authorRose, SJen_US
dc.contributor.authorMushtaq, Ten_US
dc.contributor.authorCottrell, Een_US
dc.contributor.authorMaharaj, AVen_US
dc.contributor.authorWilliams, Jen_US
dc.contributor.authorSavage, MOen_US
dc.contributor.authorMetherell, LAen_US
dc.contributor.authorStorr, HLen_US
dc.date.accessioned2020-07-14T15:49:38Z
dc.date.issued2019-09en_US
dc.identifier.issn1663-2818en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/65662
dc.format.extent111 - 111en_US
dc.language.isoenen_US
dc.rightsCC BY NC
dc.rightsAttribution-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nd/3.0/us/*
dc.titleGHR transcript heterogeneity may explain the phenotypic variability in patients with homozygous GHR pseudoexon (6 Psi) mutationen_US
dc.typeConference Proceeding
dc.rights.holder© 2020 The authors 2020
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000485922401058&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume91en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US
qmul.funderImproved genetic diagnosis of primary adrenal insufficiency::Barts Charityen_US


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