Associated Papers
A novel KRT16 frameshift variant causing pachyonychia congenita by re-initiation of translation.
Wang S et al.
Journal of the European Academy of Dermatology and Venereology : Jeadv, 2023
A KRT16 mutation in the first Chinese pedigree with Pachyonychia congenita and review of the literatures.
Xu Q et al.
Journal of Cosmetic Dermatology, 2019
A large mutational study in pachyonychia congenita.
Wilson NJ et al.
The Journal of Investigative Dermatology, 2011
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