The Role of
MCM9
Sertoli cell only syndrome
azoospermia
genetics
non-obstructive
premature ovarian failure
puberty
Journal
Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588
Informations de publication
Date de publication:
28 Jan 2023
28 Jan 2023
Historique:
received:
03
12
2022
revised:
12
01
2023
accepted:
25
01
2023
entrez:
11
2
2023
pubmed:
12
2
2023
medline:
12
2
2023
Statut:
epublish
Résumé
Infertility in couples is a common problem, with both female and male factors contributing to similar extents. Severe, congenital disorders affecting fertility are, however, rare. While folliculogenesis and spermatogenesis are generally orchestrated via different mechanisms, some genetic anomalies can impair both female and male gametogenesis. Minichromosome maintenance complex component 9 (MCM9) is involved in DNA repair and mutations of the
Identifiants
pubmed: 36769638
pii: jcm12030990
doi: 10.3390/jcm12030990
pmc: PMC9917496
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : of the Centre Hospitalier Universitaire de Liège
ID : FIRS 2020-2021
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