{
    "record_id": "PubMed.10049589", 
    "reference": {
        "url": "https://www.ncbi.nlm.nih.gov/pubmed/10049589", 
        "type": "PubMed", 
        "id": "10049589"
    }, 
    "title": "Identification and characterization of a highly conserved protein absent in the Alport syndrome (A), mental retardation (M), midface hypoplasia (M), and elliptocytosis (E) contiguous gene deletion syndrome (AMME).", 
    "journal": "Genomics", 
    "referenced_glycans": [], 
    "authors": "Pober B., Piccini M., Renieri A., Vitelli F., Caroli F., Franco B., Jonsson J., Malandrini A., Sorrentino V.", 
    "date": "1999", 
    "referenced_proteins": [
        "Q9Y4X0-1"
    ], 
    "abstract": ""
}