Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum

Clin Genet. 2011 Jan;79(1):92-5. doi: 10.1111/j.1399-0004.2010.01513.x.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Amino Acid Sequence
  • Ectodermal Dysplasia* / genetics
  • Ectodermal Dysplasia* / physiopathology
  • Exons
  • Female
  • Humans
  • Keratoderma, Palmoplantar* / genetics
  • Keratoderma, Palmoplantar* / physiopathology
  • Male
  • Molecular Sequence Data
  • Mutation*
  • Oligonucleotide Array Sequence Analysis
  • Pedigree
  • Wnt Proteins* / genetics

Substances

  • WNT10A protein, human
  • Wnt Proteins