Autosomal recessive kallmann syndrome caused by mutations in the genes encoding prokineticin 2 and prokineticin receptor 2 - Abreu, A. P.; Trarbach, E. B.; Castro, Margaret de; Costa, E. M. F.; Versiani, B.; Guerra Júnior, G.; Baptista, M. T. M.; Garmes, H. M.; Mendonça, Berenice Bilharinho de; Latronico, A. C. (Annual Meeting of the Endocrine Society, 2008)