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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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Bibliografische gegevens
Gepubliceerd in:Metabolism
Hoofdauteurs: Stamou, Maria I., Georgopoulos, Neoklis A.
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
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