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The Histopathology of PRSS1 Hereditary Pancreatitis
Hereditary pancreatitis is an autosomal dominant disorder with 80% penetrance and variable expressivity. The vast majority of cases have been linked to mutations within the cationic trypsinogen gene, also referred to as serine protease 1 (PRSS1). Other than inheritance, PRSS1 pancreatitis has been c...
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Vydáno v: | Am J Surg Pathol |
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Hlavní autoři: | , , , , , , , , , , , , , , , |
Médium: | Artigo |
Jazyk: | Inglês |
Vydáno: |
2014
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Témata: | |
On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4321743/ https://ncbi.nlm.nih.gov/pubmed/24525505 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/PAS.0000000000000164 |
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