Strong evidence that the N21I substitution in the cationic trypsinogen gene causes disease in hereditary pancreatitis

Gut. 1999 Dec;45(6):916. doi: 10.1136/gut.45.6.916.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Chronic Disease
  • Humans
  • Mutation*
  • Pancreatitis / genetics*
  • Trypsinogen / genetics*

Substances

  • Trypsinogen