{
    "PMID": "10218527",
    "TI": "Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling.",
    "JT": "Lancet (London, England)",
    "BTI": "",
    "DP": "1999-04-17",
    "AU": "Denoyelle F, Marlin S, Weil D, Moatti L, Chauvin P, Garab\u00e9dian E N, Petit C"
}
