Wordt geladen...
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...
Bewaard in:
| Gepubliceerd in: | Metabolism |
|---|---|
| Hoofdauteurs: | , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2017
|
| Onderwerpen: | |
| Online toegang: | 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 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|