3020insC mutation within the NOD2 gene in Crohn's disease: frequency and association with clinical pattern in an Italian population

Dig Liver Dis. 2002 Feb;34(2):153. doi: 10.1016/s1590-8658(02)80249-3.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Carrier Proteins / genetics*
  • Chromatography, High Pressure Liquid
  • Crohn Disease / diagnosis
  • Crohn Disease / genetics*
  • Female
  • Humans
  • Incidence
  • Intracellular Signaling Peptides and Proteins*
  • Italy
  • Male
  • Middle Aged
  • Mutation*
  • Nod2 Signaling Adaptor Protein

Substances

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