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PHENOTYPIC SPECTRUM AND RESPONSES TO RECOMBINANT HUMAN IGF-I (RHIGF-I) THERAPY IN PATIENTS WITH HOMOZYGOUS GH RECEPTOR PSEUDOEXON DEFECTS

dc.contributor.advisor© 2018 European Society of Endocrinology 2018
dc.contributor.authorChatterjee, Sen_US
dc.contributor.authorShapiro, Len_US
dc.contributor.authorRose, Sen_US
dc.contributor.authorMushtaq, Ten_US
dc.contributor.authorClayton, Pen_US
dc.contributor.authorTen, Sen_US
dc.contributor.authorBhangoo, APSen_US
dc.contributor.authorKumbattae, Uen_US
dc.contributor.authorDias, Ren_US
dc.contributor.authorMetherell, LAen_US
dc.contributor.authorSavage, MOen_US
dc.contributor.authorStorr, Hen_US
dc.date.accessioned2020-07-27T16:12:59Z
dc.date.issued2017en_US
dc.identifier.issn1663-2818en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/65841
dc.format.extent290 - 290en_US
dc.language.isoenen_US
dc.titlePHENOTYPIC SPECTRUM AND RESPONSES TO RECOMBINANT HUMAN IGF-I (RHIGF-I) THERAPY IN PATIENTS WITH HOMOZYGOUS GH RECEPTOR PSEUDOEXON DEFECTSen_US
dc.typeConference Proceeding
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000412595403161&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume88en_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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