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...

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Bibliografiska uppgifter
I publikationen:Hum Genomics
Huvudupphovsmän: 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.
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2017
Ämnen:
Primary Research
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5314676/
https://ncbi.nlm.nih.gov/pubmed/28209183
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40246-017-0098-2
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