NEMO mutational analysis in a Japanese family with incontinentia pigmenti

Eye (Lond). 2007 Jun;21(6):888-90. doi: 10.1038/sj.eye.6702770. Epub 2007 Mar 30.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • DNA Mutational Analysis
  • Eye Diseases, Hereditary / genetics*
  • Female
  • Gene Deletion
  • Humans
  • I-kappa B Kinase / genetics*
  • Incontinentia Pigmenti / genetics*
  • Infant

Substances

  • IKBKG protein, human
  • I-kappa B Kinase