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  • 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

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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

Authors

  1. Dr P Felderbauer, Department of Internal Medicine I, St Josef Hospital, Ruhr-University of Bochum, Gudrunstr. 54, 44791 Bochum, Germany; peter.felderbauer{at}rub.de
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Citation

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.

Publication history

  • Received November 27, 2007
  • Revised March 10, 2008
  • Accepted March 26, 2008
  • First published May 29, 2008.
Online issue publication 
April 27, 2016

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2008 BMJ Publishing Group