A novel 1-bp deletion mutation of the EDA gene in a Chinese Han family with X-linked hypohidrotic ectodermal dysplasia

J Dermatol. 2014 Jul;41(7):659-61. doi: 10.1111/1346-8138.12431.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Asian People / genetics
  • China
  • DNA Mutational Analysis
  • Ectodermal Dysplasia 1, Anhidrotic / genetics*
  • Ectodysplasins / genetics*
  • Exons
  • Female
  • Humans
  • Male
  • Pedigree
  • Sequence Deletion*
  • Young Adult

Substances

  • EDA protein, human
  • Ectodysplasins