Gene symbol: PRSS1. Disease: Pancreatitis, hereditary. Accession #Hm0542

Hum Genet. 2006 Feb;118(6):779.
No abstract available

MeSH terms

  • Amino Acid Substitution
  • Humans
  • Mutation, Missense
  • Pancreatitis / genetics*
  • Trypsin
  • Trypsinogen / genetics*

Substances

  • Trypsinogen
  • PRSS1 protein, human
  • Trypsin