Loss-of-function mutations in the human luteinizing hormone receptor predominantly cause intracellular retention

dc.contributor.authorNewton, Claire L.
dc.contributor.authorAnderson, Ross Calley
dc.contributor.authorKatz, Arieh Anthony
dc.contributor.authorMillar, Robert P.
dc.contributor.emailclaire.newton@up.ac.zaen_ZA
dc.date.accessioned2016-12-05T09:37:13Z
dc.date.available2016-12-05T09:37:13Z
dc.date.issued2016-11
dc.description.departmentImmunologyen_ZA
dc.description.departmentPhysiologyen_ZA
dc.description.departmentZoology and Entomologyen_ZA
dc.description.librarianam2016en_ZA
dc.description.sponsorshipThis work was supported by the South African Medical Research Council (Award to the MRC/UCT Receptor Biology Research Unit); the Claude Leon Foundation, South Africa (Postdoctoral Research Fellowship: C.L.N.); the University of Cape Town (URC Fellowship: R.C.A.); The University of Pretoria (RDP grants: C.L.N. and R.C.A.); and the National Research Foundation, South Africa (CSUR Grant [94008]: C.L.N.).en_ZA
dc.description.urihttp://press.endocrine.org/journal/endoen_ZA
dc.identifier.citationNewton, CL, Anderson, RC, Katz, AA & Millar, RP 2016, 'Loss-of-function mutations in the human luteinizing hormone receptor predominantly cause intracellular retention', Endocrinology, vol. 157, vol. 11, pp. 4364-4377.en_ZA
dc.identifier.issn0013-7227 (print)
dc.identifier.issn1945-7170 (online)
dc.identifier.other10.1210/en.2016-1104
dc.identifier.urihttp://hdl.handle.net/2263/58343
dc.language.isoenen_ZA
dc.publisherEndocrinology Societyen_ZA
dc.rights© 2016 by the Endocrine Societyen_ZA
dc.titleLoss-of-function mutations in the human luteinizing hormone receptor predominantly cause intracellular retentionen_ZA
dc.typeArticleen_ZA

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