{
    "title": "The gene encoding hydroxypyruvate reductase (GRHPR) is mutated in patients with primary hyperoxaluria type II.",
    "journal": "Human molecular genetics",
    "date": "1999",
    "authors": "Cramer SD, Ferree PM, Lin K, Milliner DS, Holmes RP",
    "reference": {
        "type": "PubMed",
        "id": "10484776",
        "url": "https://pubmed.ncbi.nlm.nih.gov/10484776"
    },
    "referenced_glycans": [],
    "referenced_proteins": [
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            "uniprot_canonical_ac": "P00505-1",
            "protein_name": "Aspartate aminotransferase, mitochondrial",
            "gene_name": "GOT2",
            "tax_name": "Human"
        },
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            "uniprot_canonical_ac": "Q14749-1",
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    ],
    "species": [
        {
            "name": "Homo sapiens",
            "taxid": 9606,
            "evidence": [
                {
                    "database": "UniProtKB",
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            "glygen_name": "Human",
            "reference_species": "Homo sapiens [9606]"
        }
    ],
    "record_id": "pubmed.10484776",
    "abstract": "",
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