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Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis

 

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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  1. doi: 10.1136/gut.50.2.271 Gut 1 February 2002 vol. 50 no. 2 271-272
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