Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2 September 1998 in “ British Journal of Dermatology ” Covello, Smith, Sillevis Smitt, Amy S. Paller, Munro, Jonkman, Uitto, W.H. Irwin McLean We don't know much about this study yet. We're maintaining the world's largest resposity of hair loss research. You can help out the community by sending a PDF of this study here . Not sure how to get a study's PDF? You can email the authors of the study. View this study on academic.oup.com →
research Mutation of a type II keratin gene (K6a) in pachyonychia congenita 232 citations , July 1995 in “Nature Genetics”
research A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21. 61 citations , September 1994 in “Journal of Medical Genetics”
research Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2 175 citations , September 1998 in “British Journal of Dermatology”
