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    {
        "title": "Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.",
        "journal": "Human molecular genetics",
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        "authors": "Bespalova IN, Van Camp G, Bom SJ, Brown DJ, Cryns K, DeWan AT, Erson AE, Flothmann K, Kunst HP, Kurnool P, Sivakumaran TA, Cremers CW, Leal SM, Burmeister M, Lesperance MM",
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        "title": "Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1.",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0010963",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0010963",
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