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A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks

Publié le 26 octobre 2023
A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks
Description
 
Date 
Auteurs
Sandrine Caburet, Anne-Laure Todeschini, Cynthia Petrillo, Emmanuelle Martini, Nada D Farran, Bérangère Legois, Gabriel Livera, Johnny S Younis, Stavit Shalev, Reiner A Veitia
Revue
Année
2019
Service
iRCM/SCSR
Institut
iRCM
Laboratoire
IRCM/SCSR/LDG
Résumé
 
Date de création30/12/2019

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