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A new polymorphism for the RI22H mutation in hereditary pancreatitis
BACKGROUND AND AIMS—Hereditary pancreatitis (HP) is a rare form of recurrent acute and chronic pancreatitis. Mutations in the cationic trypsinogen (protease serine 1, PRSS1) gene have been identified as causing HP. The R122H (previously known as R117H) mutation is the commonest and can be detected b...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2001
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1728213/ https://ncbi.nlm.nih.gov/pubmed/11156648 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/gut.48.2.247 |
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