Congenital hypogonadotropic hypogonadism due to GNRH receptor mutations in three brothers reveal sites affecting conformation and coupling

Tello, Javier A.Newton, Claire L.Bouligand, JeromeGuiochon-Mantel, AnneMillar, Robert P.Young, Jacques2012-06-252012-06-252012-06-05Tello 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.00384561932-620310.1371/journal.pone.0038456http://hdl.handle.net/2263/19240Please read abstract in article.en© 2012 Tello et al. This is an open-access article distributed under the terms of the Creative Commons Attribution LicenseCongenital hypogonadotropic hypogonadism (CHH)GnRH receptor (GNRHR1)CouplingLuteinizing hormone releasing hormoneConformational analysisMutation (Biology)Congenital hypogonadotropic hypogonadism due to GNRH receptor mutations in three brothers reveal sites affecting conformation and couplingArticle