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...

Descripción completa

Detalles Bibliográficos
Autores principales: Suzuki, Mitsuyoshi, Minowa, Kei, Nakano, Satoshi, Isayama, Hiroyuki, Shimizu, Toshiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824215/
https://www.ncbi.nlm.nih.gov/pubmed/33375361
http://dx.doi.org/10.3390/diagnostics11010031

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824215/
https://www.ncbi.nlm.nih.gov/pubmed/33375361
http://dx.doi.org/10.3390/diagnostics11010031

Ejemplares similares