{
    "record_id": "PubMed.10097181", 
    "reference": {
        "url": "https://www.ncbi.nlm.nih.gov/pubmed/10097181", 
        "type": "PubMed", 
        "id": "10097181"
    }, 
    "title": "A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca(2+) release channel function and severe central core disease.", 
    "journal": "Proc. Natl. Acad. Sci. U.S.A.", 
    "referenced_glycans": [], 
    "authors": "Tong J., MacLennan D.H., Mallet A., Giblin L., Heffron J.J.A., Lehane M., Lynch P.J., McCarthy T.V., Vaughan P., Zafra G.", 
    "date": "1999", 
    "referenced_proteins": [
        "P21817-1"
    ], 
    "abstract": ""
}