作者: J. C. Lessard , S. Pina-Paz , J. D. Rotty , R. P. Hickerson , R. L. Kaspar
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摘要: Mutations in the type I keratin 16 (Krt16) and its partner type II keratin 6 (Krt6a, Krt6b) cause pachyonychia congenita (PC), a disorder typified by dystrophic nails, painful hyperkeratotic …