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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:J Clin Res Pediatr Endocrinol
Autors principals: Akkuş, Gamze, Kotan, Leman Damla, Durmaz, Erdem, Mengen, Eda, Turan, İhsan, Ulubay, Ayça, Gürbüz, Fatih, Yüksel, Bilgin, Tetiker, Tamer, Topaloğlu, A. Kemal
Format: Artigo
Idioma:Inglês
Publicat: Galenos Publishing 2017
Matèries:
Original Article
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars