NOD2 in Crohn's disease--loss or gain of function mutations?

Neth J Med. 2005 Sep;63(8):286-7.
No abstract available

Publication types

  • Comment
  • Editorial

MeSH terms

  • Alleles
  • Animals
  • Crohn Disease / genetics*
  • Genetic Predisposition to Disease
  • Genetic Variation
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics*
  • Mice
  • Mutation*
  • Nod2 Signaling Adaptor Protein
  • Polymorphism, Single Nucleotide / genetics*

Substances

  • Intracellular Signaling Peptides and Proteins
  • NOD2 protein, human
  • Nod2 Signaling Adaptor Protein