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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發表在:Am J Surg Pathol
Main Authors: 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
格式: Artigo
語言:Inglês
出版: 2014
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Article
在線閱讀: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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