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- W2590067229 endingPage "303" @default.
- W2590067229 startingPage "283" @default.
- W2590067229 abstract "Congenital isolated hypogonadotropic hypogonadism (IHH) is a clinically and genetically heterogenous disorder characterized by abnormal synthesis, secretion, or action of gonadotropin-releasing hormone, a key hypothalamic decapeptide that orchestrates the reproductive axis. Several modes of inheritance have been identified. A growing list of causative genes has been implicated in the molecular pathogenesis of syndromic and nonsyndromic IHH, largely contributing for better understanding the complex neuroendocrine control of reproduction. This article summarizes the great advances of molecular genetics of IHH and pointed up the heterogeneity and complexity of the genetic basis of this condition." @default.
- W2590067229 created "2017-03-03" @default.
- W2590067229 creator A5004035589 @default.
- W2590067229 creator A5055317938 @default.
- W2590067229 creator A5075930640 @default.
- W2590067229 date "2017-06-01" @default.
- W2590067229 modified "2023-10-18" @default.
- W2590067229 title "Molecular and Genetic Aspects of Congenital Isolated Hypogonadotropic Hypogonadism" @default.
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