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Kallmann syndrome: phenotype and genotype of hypogonadotropic hypogonadism
Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency (IGD) IGD is a genetically and clinically heterogeneous disorder. Mutations in many different genes are able to explain ~40% of the causes of IGD, with the rest of cases remaining genetically uncharacterized. While most mutations are inherite...
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| Udgivet i: | Metabolism |
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| Main Authors: | , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2017
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5934335/ https://ncbi.nlm.nih.gov/pubmed/29108899 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.metabol.2017.10.012 |
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