Three Siblings with Idiopathic Hypogonadotropic Hypogonadism in a Nonconsanguineous Family: A Novel KISS1R/GPR54 Loss-of-Function Mutation

Idiopathic hypogonadotropic hypogonadism (IHH) is a rare disease caused by defects in the secretion of gonadotropin releasing hormone (GnRH) or the action of GnRH on the pituitary gonadotrophes. KISS1R is one of the genes which, when mutated, cause IHH and mutations of this gene are responsible for...

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Detalles Bibliográficos
Autores principales: Nalbantoğlu, Özlem, Arslan, Gülçin, Köprülü, Özge, Hazan, Filiz, Gürsoy, Semra, Özkan, Behzat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6878343/
https://www.ncbi.nlm.nih.gov/pubmed/30905142
http://dx.doi.org/10.4274/jcrpe.galenos.2019.2018.0230

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6878343/
https://www.ncbi.nlm.nih.gov/pubmed/30905142
http://dx.doi.org/10.4274/jcrpe.galenos.2019.2018.0230

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