Whole-exome sequencing identi fi es mutations in FSIP 2 as a recurrent cause of multiple morphological abnormalities of the sperm fl agella
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N. Thierry-Mieg | P. Ray | C. Coutton | R. Zouari | Selima Fourati Ben Mustapha | C. Arnoult | A. Touré | G. Martinez | M. Bidart | V. Satre | K. Pernet-Gallay | M. Bonhivers | A. Bertrand | Antoine Saut | Thomas Karaouzene | J. Hograindleur | M. Kharouf | Denis Dacheux-Deschamps | Z. Kherraf | Amir Amiri-Yekta