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                "comment": "Not a cause of male infertility.",
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    },
    {
        "title": "Missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermia.",
        "journal": "American journal of human genetics",
        "date": "2013",
        "authors": "Dirami T, Rode B, Jollivet M, Da Silva N, Escalier D, Gaitch N, Norez C, Tuffery P, Wolf JP, Becq F, Ray PF, Dulioust E, Gacon G, Bienvenu T, Toure A",
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                    {
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                        "id": "rs140210148",
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                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
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                                "description": ""
                            }
                        ],
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                    },
                    {
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                            "resource": "Disease Ontology",
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        "title": "Novel biallelic mutations in SLC26A8 cause severe asthenozoospermia in humans owing to midpiece defects: Insights into a putative dominant genetic disease.",
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