To the Editor: The studies by Goldstein and Whelan and theircolleagues (Oct. 12 issue)1,2 indicate that p16 mutations arerequired for the development of pancreatic cancer in 10 melanoma-pronekindreds in the United States, Australia, and the Netherlands,which were previously characterized with respect to chromosome9p21 by linkage analysis. We have found evidence relating therisk of pancreatic adenocarcinoma to a p16 mutation in bloodlinemembers of melanoma-prone Italian families.
So far, within a small geographic area of Italy (possibly becauseof a founder effect), we have detected the same Gly93Trp mutationin seven apparently unrelated families and . . . [Full Text of this Article]
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