Home /Research /Missense Mutations in SLC26A8, Encoding a Sperm-Specific Activator of CFTR, Are Associated with Human Asthenozoospermia
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Missense Mutations in SLC26A8, Encoding a Sperm-Specific Activator of CFTR, Are Associated with Human Asthenozoospermia

Thassadite Dirami, Baptiste Rode, M Jollivet, Nathalie Da Silva, Denise Escalier, Natacha Gaitch, Caroline Norez, Pierre Tufféry, Jean‐Philippe Wolf, Frédéric Becq, Pierre F. Ray, Emmanuel Dulioust, Gérard Gâcon, Thierry Bienvenu, Aminata Touré

Year
2013
Citations
116
Access
Open access

Keywords

AsthenozoospermiaCapacitationBiologySpermSperm motilityMissense mutationGeneticsCystic fibrosis transmembrane conductance regulatorPopulationMolecular biology

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