Mutations in gonadotropin-releasing hormone receptor gene cause hypogonadotropic hypogonadism

Idiopathic hypogonadotropic hypogonadism (IHH) is one of the most common causes of hereditary hypogonadism. Affected males and females present with irreversible pubertal delay, low serum levels of the gonadotropins follicle-stimulating hormone (FSH) and luteinizing hormone (LH), and sex steroids. Th...

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Veröffentlicht in:	Nature genetics 1998-01, Vol.18 (1), p.14-15
Hauptverfasser:	Layman, Lawrence C., Cohen, David P., Jin, Mei, Xie, Jun, Li, Zhu, Reindollar, Richard H., Bolbolan, Shahla, Bick, David P., Sherins, Richard R., Duck, L. Wayne, Musgrove, Lois C., Sellers, Jeffrey C., Neill, Jimmy D.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Agriculture Animal Genetics and Genomics Biomedical and Life Sciences Biomedicine Cancer Research correspondence Female Gene Function Human Genetics Humans Hypogonadism - genetics Male Mutation Receptors, LHRH - genetics
Online-Zugang:	Volltext
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