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
导致家族性原发性卵巢功能不全的截短型 MEIOB 突变会消除其与伴侣 SPATA22 的相互作用以及它们对 DNA 双链断裂的募集
期刊:EBioMedicine
影响因子:9.7
doi:10.1016/j.ebiom.2019.03.075
Sandrine Caburet, Anne-Laure Todeschini, Cynthia Petrillo, Emmanuelle Martini, Nada D Farran, Bérangère Legois, Gabriel Livera, Johnny S Younis, Stavit Shalev, Reiner A Veitia
