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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...

詳細記述

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書誌詳細
出版年:Am J Surg Pathol
主要な著者: 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
フォーマット: Artigo
言語:Inglês
出版事項: 2014
主題:
オンライン・アクセス: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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