You are here

  • Home
  • Archive
  • Volume 45, Issue 8
  • A novel A121T mutation in human cationic trypsinogen associated with hereditary pancreatitis: functional data indicating a loss-of-function mutation influencing the R122 trypsin cleavage site

Citation Tools

Article menu
Download PDFPDF
Original article
A novel A121T mutation in human cationic trypsinogen associated with hereditary pancreatitis: functional data indicating a loss-of-function mutation influencing the R122 trypsin cleavage site

Download to a citation manager

Download the citation for this article by clicking on one of the following citation managers:

Cite this article as:
Felderbauer P, Schnekenburger J, Lebert R, et al
A novel A121T mutation in human cationic trypsinogen associated with hereditary pancreatitis: functional data indicating a loss-of-function mutation influencing the R122 trypsin cleavage site
Journal of Medical Genetics 2008;45:507-512.