Carregant...

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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:J Clin Res Pediatr Endocrinol
Autor principal: Topaloğlu, A. Kemal
Format: Artigo
Idioma:Inglês
Publicat: Galenos Publishing 2017
Matèries:
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!