Article info
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
- 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
Citation
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
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
Article Versions
- Previous version (27 April 2016).
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2008 BMJ Publishing Group