{
    "PMID": "10070622",
    "TI": "Prenatal molecular diagnosis of severe ornithine carbamoyltransferase deficiency due to a novel mutation, E181G.",
    "JT": "Journal of inherited metabolic disease",
    "BTI": "",
    "DP": "1999-02",
    "AU": "Topaloglu A K, Sansaricq C, Fox J E, Bale A E, Tuchman M, Desnick R J"
}