{
    "PMID": "10206685",
    "TI": "The 1396del A mutation and a missense mutation or a rare polymorphism of the WRN gene detected in a French Werner family with a severe phenotype and a case of an unusual vulvar cancer. Mutations in brief no. 136. Online.",
    "JT": "Human mutation",
    "BTI": "",
    "DP": "1998",
    "AU": "Vidal V, Bay J O, Champomier F, Grancho M, Beauville L, Glowaczower C, Lemery D, Ferrara M, Bignon Y J"
}