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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:J Clin Res Pediatr Endocrinol
Egile nagusia: Topaloğlu, A. Kemal
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Galenos Publishing 2017
Gaiak:
Sarrera elektronikoa: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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