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A rare heterozygous IGFI variant causing impaired IGF-I cleavage and postnatal growth failure: a novel disease mechanism with insights into IGF-I physiology

dc.contributor.authorCottrell, Een_US
dc.contributor.authorAndrews, Aen_US
dc.contributor.authorWilliams, Jen_US
dc.contributor.authorChatterjee, Sen_US
dc.contributor.authorEdate, Sen_US
dc.contributor.authorMetherell, LAen_US
dc.contributor.authorHwa, Ven_US
dc.contributor.authorStorr, HLen_US
dc.date.accessioned2023-03-21T11:11:21Z
dc.date.issued2022en_US
dc.identifier.issn1663-2818en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/85106
dc.format.extent264 - 264en_US
dc.titleA rare heterozygous IGFI variant causing impaired IGF-I cleavage and postnatal growth failure: a novel disease mechanism with insights into IGF-I physiologyen_US
dc.typeConference Proceeding
pubs.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000854435701118&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.issueSUPPL 2en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume95en_US
qmul.funderImproved genetic diagnosis of primary adrenal insufficiency::Barts Charityen_US


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