GNRHR biallelic and digenic mutations in patients with normosmic congenital hypogonadotropic hypogonadism

Objective: Normosmic congenital hypogonadotropic hypogonadism (nCHH) is a rare disorder characterised by lack of pubertal development and infertility, due to deficient production, secretion or action of gonadotropin-releasing hormone (GnRH) and, unlike Kallmann syndrome, is associated with a normal...

Descrición completa

Detalles Bibliográficos

Principais autores:	Catarina I Gonçalves, José M Aragüés, Margarida Bastos, Luísa Barros, Nuno Vicente, Davide Carvalho, Manuel C Lemos
Formato:	Artigo
Idioma:	Inglês
Publicado:	Bioscientifica 2017-07-01
Series:	Endocrine Connections
Assuntos:	hypogonadotropic hypogonadism gonadotropin-releasing hormone GNRHR mutation genetics
Acceso en liña:	http://www.endocrineconnections.com/content/6/6/360.full
Tags:	Engadir etiqueta Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!