A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.

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

https://www.ncbi.nlm.nih.gov/pubmed/28401488

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;: