Absence of PRSS1 mutations and association of SPINK1 trypsin inhibitor mutations in hereditary and non-hereditary chronic pancreatitis

Background and aims: Mutations in the cationic trypsinogen (protease, serine, 1 (trypsin 1); PRSS1) gene are causally associated with recurrent acute and chronic pancreatitis. We investigated whether mutations in the PRSS1 gene are associated with hereditary and non-hereditary pancreatitis. As a mod...

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Hlavní autoři: Chandak, G R, Idris, M M, Reddy, D N, Mani, K R, Bhaskar, S, Rao, G V, Singh, L
Médium: Artigo
Jazyk:Inglês
Vydáno: Copyright 2004 by Gut 2004
Témata:
Pancreas
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1774044/
https://ncbi.nlm.nih.gov/pubmed/15082592
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/gut.2003.026526
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