1 Moritz DL, "Steatocystoma multiplex treated with isotretinoin: a delayed response" 42 : 437-439, 1988
2 Smith FJ, "Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex" 108 : 220-223, 1997
3 Covello SP, "Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2" 139 : 475-480, 1998
4 McLean WH, "Keratin 16 and keratin 17 mutations cause pachyonychia congenita" 9 : 273-278, 1995
5 Smith FJ, "A mutation in human keratin K6b produces a phenocopy of the K17 disorder pachyonychia congenita type 2" 7 : 1143-1148, 1998