Article info
PDFCase report
Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis
- Correspondence to:
Dr D C Whitcomb, University of Pittsburgh, 571 Scaife Hall, 3550 Terrace Street, Pittsburgh, PA 15101, USA;
whitcomb{at}pitt.edu
Citation
Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis
Publication history
- Accepted August 6, 2001
- First published February 1, 2002.
Online issue publication
October 26, 2017
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Copyright 2002 by Gut