Cargando...
Missense mutations in pancreatic secretory trypsin inhibitor (SPINK1) cause intracellular retention and degradation
BACKGROUND/AIMS: Mutations of the SPINK1 gene encoding pancreatic secretory trypsin inhibitor have been identified in association with chronic pancreatitis. The vast majority of patients carry the N34S variant, whereas other genetic variants are relatively rare and their disease association is uncer...
Gardado en:
| Main Authors: | , , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BMJ Group
2007
|
| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2000263/ https://ncbi.nlm.nih.gov/pubmed/17525091 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/gut.2006.115725 |
| Tags: |
Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|