Article
Novel <i>mutations within</i> PRSS1 Gene that could potentially cause hereditary pancreatitis: Using Comprehensive in silico Approach
2019-01-14
Abstract excerpt
<h4>Background</h4> Hereditary pancreatitis (HP) is an autosomal dominant disorder with incomplete penetrance characterized by recurring episodes of severe abdominal pain often presenting in childhood. The comprehensive in silico analysis of coding SNPs, and their functional impacts on protein level, still remains unknown. In this study, we aimed to identify the pathogenic SNPs in PRSS1 gene by computational an...
Topics
Open a Topic to create a Post that cites this publication.
Identifiers and source
- Literature Corpus work
- 94f2833f-a8aa-5b5e-ae85-8b0288302a97
- DOI
- 10.1101/519926
