Clinical characteristics and follow-up of 5 young Chinese males with gonadotropin-releasing hormone deficiency caused by mutations in the KAL1 gene

Isolated gonadotropin-releasing hormone (GnRH) deficiency (IGD) pertains to a group of genetic disorders consisting of anosmic hypogonadotropic hypogonadism (Kallmann syndrome, KS) and normosmic idiopathic hypogonadotropic hypogonadism (nIHH). KS is genetically heterogeneous. We hereby present 5 you...

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Опубликовано в: :Meta Gene
Главные авторы: Li, Juan, Li, Niu, Ding, Yu, Huang, Xiaodong, Shen, Yongnian, Wang, Jian, Wang, Xiumin
Формат: Artigo
Язык:Inglês
Опубликовано: Elsevier 2015
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Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC4707242/
https://ncbi.nlm.nih.gov/pubmed/26862482
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mgene.2015.12.001
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