Interaction between a novel intronic IVS3+ 172 variant and N29I mutation in PRSS1 gene is associated with pancreatitis in a Malaysian Chinese family
BACKGROUND/AIMS: Hereditary pancreatitis (HP) is a very rare form of early-onset chronic pancreatitis, which usually begins in childhood with a variable spectrum of severity of disease. HP is commonly caused by variants/mutations in the PRSS1 gene as reported in many studies. Therefore, in this stud...
| Main Authors: | , , , , |
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| Format: | Article |
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2011
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