Novel cationic trypsinogen (PRSS1) mutations N29T and R122C confer autosomal dominant hereditary pancreatitis
Roland H. Pluetzer, Erica S. Myerss, Suzanne E. Shapiro, Robert Finch, Ian Ellis, Jeffrey A. Kant, John P. Neoptolemos, David C. WhitcombVolume:
120
Year:
2001
Language:
english
DOI:
10.1016/s0016-5085(08)80162-x
File:
PDF, 189 KB
english, 2001