Literature DB >> 10644199

Strong evidence that the N21I substitution in the cationic trypsinogen gene causes disease in hereditary pancreatitis.

J M Chen, B Mercier, C Ferec.   

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Year:  1999        PMID: 10644199      PMCID: PMC1727754          DOI: 10.1136/gut.45.6.916

Source DB:  PubMed          Journal:  Gut        ISSN: 0017-5749            Impact factor:   23.059


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  1 in total

1.  Mutations in serine protease inhibitor Kazal type 1 are strongly associated with chronic pancreatitis.

Authors:  J P H Drenth; R te Morsche; J B M J Jansen
Journal:  Gut       Date:  2002-05       Impact factor: 23.059

  1 in total

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