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Functional effects of 13 rare PRSS1 variants presumed to cause chronic pancreatitis
OBJECTIVE: Hereditary pancreatitis is caused by mutations in human cationic trypsinogen (PRSS1) which lead to increased autoactivation by altering chymotrypsin C (CTRC)-dependent trypsinogen activation and degradation. Exceptions are some cysteine mutations which cause misfolding, intracellular rete...
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| Huvudupphovsmän: | , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2013
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3681892/ https://ncbi.nlm.nih.gov/pubmed/23455445 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/gutjnl-2012-304331 |
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