Omenn syndrome due to mutation of the RAG2 gene

J Eur Acad Dermatol Venereol. 2009 Dec;23(12):1449-51. doi: 10.1111/j.1468-3083.2009.03232.x. Epub 2009 Mar 12.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • DNA-Binding Proteins / genetics*
  • Female
  • Humans
  • Infant, Newborn
  • Mutation*
  • Nuclear Proteins / genetics*
  • Severe Combined Immunodeficiency / genetics*

Substances

  • DNA-Binding Proteins
  • Nuclear Proteins
  • RAG2 protein, human