CARD 15 / NOD 2 in paediatric onset Crohn's disease

J Pediatr Gastroenterol Nutr. 2004 Aug;39(2):216. doi: 10.1097/00005176-200408000-00024.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Crohn Disease / genetics*
  • Gene Frequency
  • Genotype
  • Humans
  • Mutation*
  • Phenotype