{
    "title": "Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus.",
    "journal": "Nature genetics",
    "date": "1999",
    "authors": "Yamamoto H, Simon A, Eriksson U, Harris E, Berson EL, Dryja TP",
    "reference": {
        "type": "PubMed",
        "id": "10369264",
        "url": "https://pubmed.ncbi.nlm.nih.gov/10369264"
    },
    "referenced_glycans": [],
    "referenced_proteins": [
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            "uniprot_canonical_ac": "P12271-1",
            "protein_name": "Retinaldehyde-binding protein 1",
            "gene_name": "RLBP1",
            "tax_name": "Human"
        },
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            "uniprot_canonical_ac": "Q8NBN7-1",
            "protein_name": "Retinol dehydrogenase 13",
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            "tax_name": "Human"
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            "protein_name": "Long-wave-sensitive opsin 1",
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            "protein_name": "Lecithin retinol acyltransferase",
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        },
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        },
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        },
        {
            "uniprot_canonical_ac": "Q96NR8-1",
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        },
        {
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            "tax_name": "Human"
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            "name": "Homo sapiens",
            "taxid": 9606,
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            "glygen_name": "Human",
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