Variants in congenital hypogonadotrophic hypogonadism genes identified in an Indonesian cohort of 46,XY under-virilised boys

BACKGROUND: Congenital hypogonadotrophic hypogonadism (CHH) and Kallmann syndrome (KS) are caused by disruption to the hypothalamic-pituitary-gonadal (H-P-G) axis. In particular, reduced production, secretion or action of gonadotrophin-releasing hormone (GnRH) is often responsible. Various genes, ma...

Descripción completa

Detalles Bibliográficos
Autores principales: Ayers, Katie L., Bouty, Aurore, Robevska, Gorjana, van den Bergen, Jocelyn A., Juniarto, Achmad Zulfa, Listyasari, Nurin Aisyiyah, Sinclair, Andrew H., Faradz, Sultana M. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Primary Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5314676/
https://www.ncbi.nlm.nih.gov/pubmed/28209183
http://dx.doi.org/10.1186/s40246-017-0098-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5314676/
https://www.ncbi.nlm.nih.gov/pubmed/28209183
http://dx.doi.org/10.1186/s40246-017-0098-2

Ejemplares similares