{
    "record_id": "PubMed.10071056", 
    "reference": {
        "url": "https://www.ncbi.nlm.nih.gov/pubmed/10071056", 
        "type": "PubMed", 
        "id": "10071056"
    }, 
    "title": "The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype.", 
    "journal": "Brain", 
    "referenced_glycans": [], 
    "authors": "Ceuterick C., Van Broeckhoven C., De Jonghe P., De Vriendt E., Nelis E., Timmerman V., Van Maldergem L., Verellen C., Martin J.-J., Lofgren A., Vercruyssen A.", 
    "date": "1999", 
    "referenced_proteins": [
        "P25189-1"
    ], 
    "abstract": ""
}