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Autor:
Bruno Leheup, Marc Klein, V. Pascal-Vigneron, Georges Weryha, Thomas Cuny, Céline Bonnet, M. Agopiantz, Arthur Sorlin, Philippe Jonveaux, P. Corbonnois, N. Hubert
Publikováno v:
Journal of Endocrinological Investigation
Journal of Endocrinological Investigation, Editrice Kurtis, 2014, 37 (1), pp.1-7. ⟨10.1007/s40618-013-0001-5⟩
Journal of Endocrinological Investigation, Editrice Kurtis, 2014, 37 (1), pp.1-7. ⟨10.1007/s40618-013-0001-5⟩
International audience; First described in 1983, Woodhouse-Sakati syndrome (WSS) is a rare autosomal recessive genetic disorder that leads to a spectrum of hypogonadal symptoms in adolescence. The responsible gene, DCAF17 located on chromosome 2q31.1