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dc.contributor.authorZhou, J
dc.contributor.authorBoulkroun, S
dc.contributor.authorCabrera, CP
dc.contributor.authorAzizan, EAB
dc.contributor.authorFernandes-Rosa, F
dc.contributor.authorCottrell, E
dc.contributor.authorArgentesi, G
dc.contributor.authorWu, X
dc.contributor.authorO’Toole, S
dc.contributor.authorMarker, A
dc.contributor.authorJordan, S
dc.contributor.authorBerney, DM
dc.contributor.authorLines, K
dc.contributor.authorMetherell, L
dc.contributor.authorTeo, A
dc.contributor.authorThakker, RV
dc.contributor.authorDrake, W
dc.contributor.authorWozniak, E
dc.contributor.authorMein, CA
dc.contributor.authorStorr, HL
dc.contributor.authorZennaro, M-C
dc.contributor.authorBrown, MJ
dc.date.accessioned2021-05-17T17:35:22Z
dc.date.available2021-05-17T17:35:22Z
dc.date.issued2021-05-03
dc.identifier.issn2472-1972
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/71887
dc.format.extenta65 - a66
dc.publisherOxford University Pressen_US
dc.relation.ispartofJournal of the Endocrine Society
dc.titleCTNNB1-Mutant Aldosterone-Producing Adenomas With Somatic Mutations of GNA11/GNAQ Have Distinct Phenotype and Genotypeen_US
dc.typeArticleen_US
dc.identifier.doi10.1210/jendso/bvab048.133
pubs.issueSupplement_1en_US
pubs.notesNot knownen_US
pubs.volume5en_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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