A new KRT86 mutation in a Chinese family with monilethrix

Clin Exp Dermatol. 2022 Feb;47(2):461-463. doi: 10.1111/ced.14956. Epub 2021 Nov 23.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Asian People
  • Child, Preschool
  • DNA Mutational Analysis
  • Female
  • Gene Deletion*
  • Heterozygote
  • Humans
  • Keratins, Hair-Specific / genetics*
  • Keratins, Type II / genetics*
  • Monilethrix / genetics*

Substances

  • KRT86 protein, human
  • Keratins, Hair-Specific
  • Keratins, Type II