{
    "PMID": "10407773",
    "TI": "A review of biochemical and molecular genetic aspects of tyrosine hydroxylase deficiency including a novel mutation (291delC).",
    "JT": "Journal of inherited metabolic disease",
    "BTI": "",
    "DP": "1999-06",
    "AU": "Wevers R A, de Rijk-van Andel J F, Br\u00e4utigam C, Geurtz B, van den Heuvel L P, Steenbergen-Spanjers G C, Smeitink J A, Hoffmann G F, Gabre\u00ebls F J"
}