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Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations
OBJECTIVE: The underlying genetic etiology of hypogonadotropic hypogonadism (HH) is heterogeneous. Fibroblast growth factor signaling is pivotal in the ontogeny of gonadotropin-releasing hormone neurons. Loss-of-function mutations in FGFR1 gene cause variable HH phenotypes encompassing pubertal dela...
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| 出版年: | J Clin Res Pediatr Endocrinol |
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| 主要な著者: | , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Galenos Publishing
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5463295/ https://ncbi.nlm.nih.gov/pubmed/28008864 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/jcrpe.3908 |
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