Missense Mutations in Keratin 17 Cause Either Pachyonychia Congenita Type 2 or a Phenotype Resembling Steatocystoma Multiplex.
Smith, 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., Lane, E. BirgVolume:
108
Pages:
4
Journal:
Journal of Investigative Dermatology
DOI:
10.1111/1523-1747.ep12335315
Date:
February, 1997
File:
PDF, 1.16 MB
1997