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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Bibliografski detalji
Izdano u:Am J Surg Pathol
Glavni autori: Singhi, Aatur D., Pai, Reetesh K., Kant, Jeffrey A., Bartholow, Tanner L., Zeh, Herbert J., Lee, Kenneth K., Wijkstrom, Martin, Yadav, Dhiraj, Bottino, Rita, Brand, Randall E., Chennat, Jennifer S., Lowe, Mark E., Papachristou, Georgios I., Slivka, Adam, Whitcomb, David C., Humar, Abhinav
Format: Artigo
Jezik:Inglês
Izdano: 2014
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Article
Online pristup: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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