{
    "PMID": "10647719",
    "TI": "Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclase.",
    "JT": "Ophthalmology",
    "BTI": "",
    "DP": "2000-01",
    "AU": "Gregory-Evans K, Kelsell R E, Gregory-Evans C Y, Downes S M, Fitzke F W, Holder G E, Simunovic M, Mollon J D, Taylor R, Hunt D M, Bird A C, Moore A T"
}
