[
    {
        "title": "Homozygous dystroglycan mutation associated with a novel muscle-eye-brain disease-like phenotype with multicystic leucodystrophy.",
        "journal": "Neurogenetics",
        "date": "2013",
        "authors": "Geis T, Marquard K, Rodl T, Reihle C, Schirmer S, von Kalle T, Bornemann A, Hehr U, Blankenburg M",
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        "title": "DAG1 mutations associated with asymptomatic hyperCKemia and hypoglycosylation of alpha-dystroglycan.",
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                            {
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                                "id": "MONDO:0013440",
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                                "resource": "MIM",
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                                "id": "DOID:0110293",
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                            {
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                                "id": "DOID:0111232",
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