Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella

Martinez, Guillaume; Kherraf, Zine-Eddine; Zouari, Raoudha; Fourati Ben Mustapha, Selima; Saut, Antoine; Pernet-Gallay, Karin; Bertrand, Anne; Bidart, Marie; Hograindleur, Jean Pascal; Amiri-Yekta, Amir; Kharouf, Mahmoud; Karaouzène, Thomas; Thierry-Mieg, Nicolas; Dacheux-Deschamps, Denis; Satre, Véronique; Bonhivers, Mélanie; Touré, Aminata; Arnoult, Christophe; Ray, Pierre F; Coutton, Charles