A recurrent intragenic deletion in the desmoglein 4 gene underlies localized autosomal recessive hypotrichosis

J Invest Dermatol. 2004 Sep;123(3):607-10. doi: 10.1111/j.0022-202X.2004.23311.x.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cadherins / genetics*
  • Child
  • Child, Preschool
  • Cytoskeletal Proteins / genetics*
  • Desmogleins
  • Female
  • Gene Deletion*
  • Humans
  • Hypotrichosis / genetics*
  • Pedigree

Substances

  • Cadherins
  • Cytoskeletal Proteins
  • DSG4 protein, human
  • Desmogleins