Cite
HARVARD Citation
Pfützer, R. et al. (2002). Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis. Gut. 50 (2), pp. 271-272. [Online].
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Pfützer, R. et al. (2002). Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis. Gut. 50 (2), pp. 271-272. [Online].