1. 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. Issue 8 (29th May 2008) Authors: Felderbauer, P; Schnekenburger, J; Lebert, R; Bulut, K; Parry, M; Meister, T; Schick, V; Schmitz, F; Domschke, W; Schmidt, W E Journal: Journal of medical genetics Issue: Volume 45:Issue 8(2008) Page Start: 507 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗