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Update on the Genetics of Idiopathic Hypogonadotropic Hypogonadism
Traditionally, idiopathic hypogonadotropic hypogonadism (IHH) is divided into two major categories: Kallmann syndrome (KS) and normosmic IHH (nIHH). To date, inactivating variants in more than 50 genes have been reported to cause IHH. These mutations are estimated to account for up to 50% of all app...
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| Publicado en: | J Clin Res Pediatr Endocrinol |
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| Autor Principal: | |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Galenos Publishing
2017
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5790323/ https://ncbi.nlm.nih.gov/pubmed/29280744 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/jcrpe.2017.S010 |
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