{
    "PMID": "10200051",
    "TI": "Gorlin syndrome: identification of 4 novel germ-line mutations of the human patched (PTCH) gene. Mutations in brief no. 137. Online.",
    "JT": "Human mutation",
    "BTI": "",
    "DP": "1998",
    "AU": "Hasenpusch-Theil K, Bataille V, Laehdetie J, Obermayr F, Sampson J R, Frischauf A M"
}