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One or more keywords matched the following properties of A novel p.Ser282Pro CPA1 variant is associated with autosomal dominant hereditary pancreatitis.

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has major subject area list Pancreatitis, Chronic; Trypsin Inhibitor, Kazal Pancreatic
has minor subject area list Chronic Disease; Humans; Mutation; Pancreatitis; Trypsin; Trypsinogen
information resource reference Kujko AA, Berki DM, Oracz G, Wejnarska K, Antoniuk J, Wertheim-Tysarowska K, Kolodziejczyk E, Bal J, Sahin-Tóth M, Rygiel AM. A novel p.Ser282Pro CPA1 variant is associated with autosomal dominant hereditary pancreatitis. Gut. 2017 09; 66(9):1728-1730. PMID: 28258133.
label A novel p.Ser282Pro CPA1 variant is associated with autosomal dominant hereditary pancreatitis.

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  • Pancreatitis