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Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis
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  1. Correspondence to:
    Dr D C Whitcomb, University of Pittsburgh, 571 Scaife Hall, 3550 Terrace Street, Pittsburgh, PA 15101, USA;
    whitcomb{at}pitt.edu
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Citation

Pfützer R, Myers E, Applebaum-Shapiro S, et al
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 
February 01, 2002
  •  

    Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis
    R Pfützer, E Myers, S Applebaum-Shapiro, R Finch, I Ellis, J Neoptolemos, J A Kant, and D C Whitcomb
    Gut 2002; 50: 271-272.

    This paper was originally published in the February issue of Gut in a condensed form.

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