Familial isolated acanthosis nigricans as a result of a recurrent FGFR3 truncating mutation

Clin Exp Dermatol. 2023 Jun 5;48(6):729-732. doi: 10.1093/ced/llad078.
No abstract available

MeSH terms

  • Acanthosis Nigricans* / genetics
  • Humans
  • Mutation
  • Receptor, Fibroblast Growth Factor, Type 3 / genetics

Substances

  • FGFR3 protein, human
  • Receptor, Fibroblast Growth Factor, Type 3

Supplementary concepts

  • Familial acanthosis nigricans