GnRH
POU6f2 isoform1
idiopathic hypogonadotropic hypogonadism
puberty
transcription
Journal
Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782
Informations de publication
Date de publication:
2023
2023
Historique:
received:
10
04
2023
accepted:
23
06
2023
medline:
22
8
2023
pubmed:
21
8
2023
entrez:
21
8
2023
Statut:
epublish
Résumé
Idiopathic hypogonadotropic hypogonadism (IHH) is characterized by the absence of pubertal development and subsequent impaired fertility often due to gonadotropin-releasing hormone (GnRH) deficits. Exome sequencing of two independent cohorts of IHH patients identified 12 rare missense variants in
Identifiants
pubmed: 37600690
doi: 10.3389/fendo.2023.1203542
pmc: PMC10436210
doi:
Substances chimiques
Gonadotropin-Releasing Hormone
33515-09-2
POU Domain Factors
0
POU6F2 protein, human
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1203542Informations de copyright
Copyright © 2023 Cho, Gurbuz, Stamou, Kotan, Farmer, Can, Tompkins, Mammadova, Altincik, Gokce, Catli, Bugrul, Bartlett, Turan, Balasubramanian, Yuksel, Seminara, Wray and Topaloglu.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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