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Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism
Idiopathic hypogonadotropic hypogonadism (IHH) due to defects of gonadotropin-releasing hormone (GnRH) secretion and/or action is a developmental disorder of sexual maturation. To date, several single-gene defects have been implicated in the pathogenesis of IHH. However, significant inter- and intra...
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
American Society for Clinical Investigation
2007
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1765517/ https://ncbi.nlm.nih.gov/pubmed/17235395 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI29884 |
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