Congenital hypogonadotropic hypogonadism due to GNRH receptor mutations in three brothers reveal sites affecting conformation and coupling
| dc.contributor.author | Tello, Javier A. | |
| dc.contributor.author | Newton, Claire L. | |
| dc.contributor.author | Bouligand, Jerome | |
| dc.contributor.author | Guiochon-Mantel, Anne | |
| dc.contributor.author | Millar, Robert P. | |
| dc.contributor.author | Young, Jacques | |
| dc.date.accessioned | 2012-06-25T06:46:01Z | |
| dc.date.available | 2012-06-25T06:46:01Z | |
| dc.date.issued | 2012-06-05 | |
| dc.description.abstract | Please read abstract in article. | en |
| dc.description.librarian | nf2012 | en |
| dc.description.sponsorship | The work was supported by the Medical Research Council, UK and by institutional grants from Universite´ Paris-Sud (Bonus Qualite´ Recherche), Institut National de la Sante´ et de la Recherche Me´dicale (INSERM), Agence Nationale de la Recherche Genopath (ANR KALGENOPATH), Fondation pour la Recherche Me´dicale (FRM), Programme Hospitalier de Recherche Clinique (PHRC). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. | en_US |
| dc.description.uri | http://www.plosone.org | en_US |
| dc.identifier.citation | Tello JA, Newton CL, Bouligand J, Guiochon-Mantel A, Millar RP, et al. (2012) Congenital Hypogonadotropic Hypogonadism Due to GNRH Receptor Mutations in Three Brothers Reveal Sites Affecting Conformation and Coupling. PLoS ONE 7(6): e38456. DOI:10.1371/journal.pone.0038456 | en |
| dc.identifier.issn | 1932-6203 | |
| dc.identifier.other | 10.1371/journal.pone.0038456 | |
| dc.identifier.uri | http://hdl.handle.net/2263/19240 | |
| dc.language.iso | en | en_US |
| dc.publisher | Public Library of Science | en_US |
| dc.rights | © 2012 Tello et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License | en_US |
| dc.subject | Congenital hypogonadotropic hypogonadism (CHH) | en |
| dc.subject | GnRH receptor (GNRHR1) | en |
| dc.subject | Coupling | en |
| dc.subject.lcsh | Luteinizing hormone releasing hormone | en |
| dc.subject.lcsh | Conformational analysis | en |
| dc.subject.lcsh | Mutation (Biology) | en |
| dc.title | Congenital hypogonadotropic hypogonadism due to GNRH receptor mutations in three brothers reveal sites affecting conformation and coupling | en |
| dc.type | Article | en |