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Caburet, S., Todeschini, A.-L., Petrillo, C., Martini, E., Farran, N. D., Legois, B., … Veitia, R. A. (2019). 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. EBioMedicine. doi:10.1016/j.ebiom.2019.03.075 
10.1016/j.ebiom.2019.03.075
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