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Genetic Abnormalities in Pancreatitis: An Update on Diagnosis, Clinical Features, and Treatment
Several pancreatitis susceptibility genes have been identified to date. A relationship between a mutation in the cationic trypsinogen (protease serine 1, PRSS1) gene and hereditary pancreatitis (HP) was first identified in 1996. Currently, HP has been defined as either two or more individuals within...
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| Izdano u: | Diagnostics (Basel) |
|---|---|
| Glavni autori: | , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
MDPI
2020
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7824215/ https://ncbi.nlm.nih.gov/pubmed/33375361 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/diagnostics11010031 |
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