A functional spectrum of PROKR2 mutations identified in isolated hypogonadotropic hypogonadism.
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DOI: 10.1093/hmg/ddad014
Abstract: Isolated hypogonadotropic hypogonadism (IHH) is a rare disease with hypogonadism and infertility caused by the defects in embryonic migration of hypothalamic gonadotropin-releasing hormone (GnRH) neurons, hypothalamic GnRH secretion or GnRH signal transduction. PROKR2 gene, encoding… read more here.
Keywords: prokr2 mutations; isolated hypogonadotropic; hypogonadotropic hypogonadism; prokr2 ... See more keywords