A recurrent intragenic deletion mutation in DSG4 gene in three Pakistani families with autosomal recessive hypotrichosis

J Invest Dermatol. 2004 Jul;123(1):247-8. doi: 10.1111/j.0022-202X.2004.22715.x.
No abstract available

Publication types

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

MeSH terms

  • Cadherins / genetics*
  • Cytoskeletal Proteins / genetics*
  • Desmogleins
  • Family Health
  • Gene Deletion*
  • Genes, Recessive
  • Humans
  • Hypotrichosis / genetics*
  • Pakistan

Substances

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