A mutation in human keratin K6b produces a phenocopy of the K17 disorder pachyonychia congenita type 2.
Smith, Frances J. D.; Jonkman, Marcel F.; van Goor, Harry; Coleman, Carrie M.; Covello, Seana P.; Uitto, Jouni; McLean, W. H. Irwin; Human Molecular Genetics, 1998, vol. 7, issue 7, p 1143, ISSN 09646906. ISBN 09646906.

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