Missense Mutations in Keratin 17 Cause Either Pachyonychia Congenita Type 2 or a Phenotype Resembling Steatocystoma Multiplex
Titel:
Missense Mutations in Keratin 17 Cause Either Pachyonychia Congenita Type 2 or a Phenotype Resembling Steatocystoma Multiplex
Auteur:
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. Birgitte Lane, E. Irwin McLean, W.H.