We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMissense Mutations in Keratin 17 Cause Either Pachyonychia Congenita Type 2 or a Phenotype Resembling Steatocystoma MultiplexAuthorsSmith, Frances J.D.; Corden, Laura D.; Rugg, Elizabeth L.; Ratnavel, Ravi; Leigh, Irene M.; Moss, Celia; Tidman, Michael J.; Hohl, Daniel; Huber, Marcel; Kunkeler, Lia; Munro, Colin S.; Birgitte Lane, E.; Irwin McLean, W.H.PublicationJournal of Investigative Dermatology, 1997, Vol 108, Issue 2, p220ISSN0022-202xPublication typearticleDOI10.1111/1523-1747.ep12335315