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

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dc.contributor.author Newton, Claire L.
dc.contributor.author Anderson, Ross Calley
dc.contributor.author Katz, Arieh Anthony
dc.contributor.author Millar, Robert P.
dc.date.accessioned 2016-12-05T09:37:13Z
dc.date.available 2016-12-05T09:37:13Z
dc.date.issued 2016-11
dc.description.department Immunology en_ZA
dc.description.department Physiology en_ZA
dc.description.department Zoology and Entomology en_ZA
dc.description.librarian am2016 en_ZA
dc.description.sponsorship This 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.uri http://press.endocrine.org/journal/endo en_ZA
dc.identifier.citation Newton, 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.issn 0013-7227 (print)
dc.identifier.issn 1945-7170 (online)
dc.identifier.other 10.1210/en.2016-1104
dc.identifier.uri http://hdl.handle.net/2263/58343
dc.language.iso en en_ZA
dc.publisher Endocrinology Society en_ZA
dc.rights © 2016 by the Endocrine Society en_ZA
dc.title Loss-of-function mutations in the human luteinizing hormone receptor predominantly cause intracellular retention en_ZA
dc.type Article en_ZA


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