Entire PTCH1 deletion is a common event in point mutation-negative cases with nevoid basal cell carcinoma syndrome in Japan

Clin Genet. 2011 Feb;79(2):196-8. doi: 10.1111/j.1399-0004.2010.01527.x.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Basal Cell Nevus Syndrome / genetics*
  • Child
  • Child, Preschool
  • Female
  • Gene Deletion*
  • Humans
  • Infant
  • Japan
  • Male
  • Patched Receptors
  • Patched-1 Receptor
  • Receptors, Cell Surface / genetics*

Substances

  • PTCH1 protein, human
  • Patched Receptors
  • Patched-1 Receptor
  • Receptors, Cell Surface