Loss-of-function mutations in the human luteinizing hormone receptor predominantly cause intracellular retention
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.contributor.email | claire.newton@up.ac.za | en_ZA |
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 |