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GnRH Deficient Patients With Congenital Hypogonadotropic Hypogonadism: Novel Genetic Findings in ANOS1, RNF216, WDR11, FGFR1, CHD7, and POLR3A Genes in a Case Series and Review of the Literature

Background: Congenital hypogonadotropic hypogonadism (CHH) is a rare genetic disease caused by Gonadotropin-Releasing Hormone (GnRH) deficiency. So far a limited number of variants in several genes have been associated with the pathogenesis of the disease. In this original research and review manusc...

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Detalles Bibliográficos
Autores principales:	Neocleous, Vassos, Fanis, Pavlos, Toumba, Meropi, Tanteles, George A., Schiza, Melpo, Cinarli, Feride, Nicolaides, Nicolas C., Oulas, Anastasis, Spyrou, George M., Mantzoros, Christos S., Vlachakis, Dimitrios, Skordis, Nicos, Phylactou, Leonidas A.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2020
Materias:	Endocrinology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7485345/ https://www.ncbi.nlm.nih.gov/pubmed/32982993 http://dx.doi.org/10.3389/fendo.2020.00626

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