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

✍ Scribed by Roland H. Pluetzer; Erica S. Myerss; Suzanne E. Shapiro; Robert Finch; Ian Ellis; Jeffrey A. Kant; John P. Neoptolemos; David C. Whitcomb

Book ID: 119429029
Publisher: Elsevier Science
Year: 2001
Tongue: English
Weight: 189 KB
Volume: 120
Category: Article
ISSN: 0016-5085
DOI: 10.1016/s0016-5085(08)80162-x

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