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ArticleThe Journal of urology2014

Re: missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermia.

Anthony AtalaPubMed ↗Publisher ↗

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Re: missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermia. | OpenQuestion