A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.
Fiche publication
Date publication
avril 2017
Journal
Journal of assisted reproduction and genetics
Auteurs
Membres identifiés du Cancéropôle Est :
Dr LAMOUR Valérie, Dr TELETIN Marius, Pr VIVILLE Stéphane, Dr CHARLET BERGUERAND Nicolas
Tous les auteurs :
Okutman O, Muller J, Skory V, Garnier JM, Gaucherot A, Baert Y, Lamour V, Serdarogullari M, Gultomruk M, Röpke A, Kliesch S, Herbepin V, Aknin I, Benkhalifa M, Teletin M, Bakircioglu E, Goossens E, Charlet-Berguerand N, Bahceci M, Tüttelmann F, Viville S
Lien Pubmed
Résumé
The purpose of this study was to identify mutations that cause non-syndromic male infertility using whole exome sequencing of family cases.
Mots clés
Azoospermia, MAGEB4, Male infertility, No-stop mutations, Oligozoospermia, Whole exome sequencing
Référence
J. Assist. Reprod. Genet.. 2017 Apr;: