{
    "record_id": "PubMed.10080186", 
    "reference": {
        "url": "https://www.ncbi.nlm.nih.gov/pubmed/10080186", 
        "type": "PubMed", 
        "id": "10080186"
    }, 
    "title": "Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1.", 
    "journal": "Nat. Genet.", 
    "referenced_glycans": [], 
    "authors": "Johnson C., Aminoff M., Broch H., Moestrup S.K., de la Chapelle A., Krahe R., Abdelaal M.A., Carter J.E., Chadwick R.B., Graesbeck R., Jenner L.B., Verroust P.J.", 
    "date": "1999", 
    "referenced_proteins": [
        "O60494-1"
    ], 
    "abstract": ""
}