Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism

Date
2012
Author
Mengen, Eda
BERBEROĞLU, MERİH
Ozbek, Mehmet Nuri
Demirbilek, Huseyin
Kekil, M. Burcu
Temiz, Fatih
Mungan, Neslihan Onenli
YÜKSEL, BİLGİN
TOPALOĞLU, ALİ KEMAL
Saka, Nurcin
Guven, Ayla
Poyrazoglu, Sukran
GÜRBÜZ, FATİH
KOTAN, LEMAN DAMLA
ŞIKLAR, ZEYNEP
Dokmetas, Sebila
Kilicli, Mehmet Fatih
KİREL, BİRGÜL
Cesur, Yasar
Dogan, Murat
Ozen, Samim
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Abstract
Objective: Normosmic idiopathic hypogonadotropic hypogonadism (nIHH) is characterized by failure of initiation or maintenance of puberty due to insufficient gonadotropin release, which is not associated with anosmia/hyposmia. The objective of this study was to determine the distribution of causative mutations in a hereditary form of nIHH.
URI
http://hdl.handle.net/20.500.12627/167337
https://doi.org/10.4274/jcrpe.725
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