{
    "PMID": "10400990",
    "TI": "An L1 element intronic insertion in the black-eyed white (Mitf[mi-bw]) gene: the loss of a single Mitf isoform responsible for the pigmentary defect and inner ear deafness.",
    "JT": "Human molecular genetics",
    "BTI": "",
    "DP": "1999-08",
    "AU": "Yajima I, Sato S, Kimura T, Yasumoto K, Shibahara S, Goding C R, Yamamoto H"
}
