{
    "PMID": "10049589",
    "TI": "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).",
    "JT": "Genomics",
    "BTI": "",
    "DP": "1999-02-01",
    "AU": "Vitelli F, Piccini M, Caroli F, Franco B, Malandrini A, Pober B, Jonsson J, Sorrentino V, Renieri A"
}