A mutation in human keratin K6b produces a phenocopy of the K17 disorder pachyonychia congenita type 2.
Smith FJ; Jonkman MF; van Goor H; Coleman CM; Covello SP; Uitto J; McLean WH; Human Molecular Genetics, 1998, vol. 7, issue 7, p 1143, ISSN 09646906. ISBN 09646906.

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