{
    "PMID": "10521293",
    "TI": "Clinical and molecular genetic analysis of 19 Wolfram syndrome kindreds demonstrating a wide spectrum of mutations in WFS1.",
    "JT": "American journal of human genetics",
    "BTI": "",
    "DP": "1999-11",
    "AU": "Hardy C, Khanim F, Torres R, Scott-Brown M, Seller A, Poulton J, Collier D, Kirk J, Polymeropoulos M, Latif F, Barrett T"
}