Defective AMH signaling disrupts GnRH neuron development and function and contributes to hypogonadotropic hypogonadism
<jats:p>Congenital hypogonadotropic hypogonadism (CHH) is a condition characterized by absent puberty and infertility due to gonadotropin releasing hormone (GnRH) deficiency, which is often associated with anosmia (Kallmann syndrome, KS). We identified loss-of-function heterozygous mutations i...
| 主要な著者: | , , , , , , , , , , , , , , , , , , , |
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| フォーマット: | Journal article |
| 言語: | English |
| 出版事項: |
eLife Publications
2019
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