{
    "PMID": "10587579",
    "TI": "Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss.",
    "JT": "Human molecular genetics",
    "BTI": "",
    "DP": "2000-01-01",
    "AU": "Liu X Z, Xia X J, Xu L R, Pandya A, Liang C Y, Blanton S H, Brown S D, Steel K P, Nance W E"
}