A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency
FANCM纯合突变是家族性非综合征型原发性卵巢功能不全的根本原因。
期刊:Elife
影响因子:6.4
doi:10.7554/eLife.30490
Baptiste Fouquet # ,Patrycja Pawlikowska # ,Sandrine Caburet ,Celine Guigon ,Marika Mäkinen ,Laura Tanner ,Marja Hietala ,Kaja Urbanska ,Laura Bellutti ,Bérangère Legois ,Bettina Bessieres ,Alain Gougeon ,Alexandra Benachi ,Gabriel Livera ,Filippo Rosselli ,Reiner A Veitia # ,Micheline Misrahi #