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dc.contributor.authorSmith, Cen_US
dc.contributor.authorRead, Jen_US
dc.contributor.authorHall, Cen_US
dc.contributor.authorMaharaj, Aen_US
dc.contributor.authorMarroquin, RLen_US
dc.contributor.authorQamar, Yen_US
dc.contributor.authorHughes, Cen_US
dc.contributor.authorClark, Aen_US
dc.contributor.authorPrasad, Ren_US
dc.contributor.authorChan, Len_US
dc.contributor.authorMusa, Sen_US
dc.contributor.authorMetherell, Len_US
dc.date.accessioned2023-03-21T11:12:38Z
dc.identifier.issn1470-3947en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/85108
dc.publisherBioscientificaen_US
dc.relation.ispartofEndocrine Abstractsen_US
dc.titleA rapid genetic diagnosis for >80% individuals with non-CAH Primary Adrenal Insufficiency is achievable by candidate gene sequencing combined with WESen_US
dc.typeArticle
dc.identifier.doi10.1530/endoabs.81.rc2.1en_US
pubs.notesNot knownen_US
qmul.funderImproved genetic diagnosis of primary adrenal insufficiency::Barts Charityen_US
qmul.funderImproved genetic diagnosis of primary adrenal insufficiency::Barts Charityen_US
qmul.funderImproved genetic diagnosis of primary adrenal insufficiency::Barts Charityen_US


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