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
Titel:
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
Auteur:
Caburet, Sandrine Todeschini, Anne-Laure Petrillo, Cynthia Martini, Emmanuelle Farran, Nada D. Legois, Bérangère Livera, Gabriel Younis, Johnny S. Shalev, Stavit Veitia, Reiner A.