Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis (Q28344965)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis |
scientific article |
Statements
Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis (English)
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February 2002
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50
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2
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271-2
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