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; et al. (Human reproduction (Oxford), 2018)
Keywords: Adult; Case-Control Studies; Humans; Infertility, Male - genetics; Life Sciences; Male; Middle Aged; Mutation; Quantitative Methods; Real-Time Polymerase Chain Reaction; Retrospective Studies; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Sperm Tail - pathology; Sperm Tail - ultrastructure; Teratozoospermia - diagnosis; Teratozoospermia - genetics; Whole Exome Sequencing - methods; fibrous sheath; multiple morphological abnormalities of the sperm flagella; flagellum; gene mutation; genetic diagnosis; male infertility; whole-exome sequencing