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

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Publication | Open Access

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

DOI Full Paper Access

114

Citations

23

References

2013

Year

Thassadite Dirami, Baptiste Rode, M Jollivet, Nathalie Da Silva, Denise Escalier, Natacha Gaitch, Caroline Norez, Pierre Tufféry, Jean‐Philippe Wolf, Frédéric Becq,

The American Journal of Human Genetics

InfertilityMissense MutationsDevelopmental BiologyGenetic DisorderGeneticsGameteMolecular GeneticsReproductive BiologyHuman AsthenozoospermiaSperm-specific ActivatorMedicineHuman Reproduction

References

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