A novel KRT6A mutation in a case of pachyonychia congenita from India

Indian J Dermatol Venereol Leprol. 2017 Jan-Feb;83(1):95-98. doi: 10.4103/0378-6323.193620.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adolescent
  • Female
  • Humans
  • India
  • Keratin-6 / genetics*
  • Mutation / genetics*
  • Pachyonychia Congenita / diagnosis*
  • Pachyonychia Congenita / genetics*
  • Pedigree

Substances

  • KRT6A protein, human
  • Keratin-6