Two novel severe mutations in the pancreatic secretory trypsin inhibitor gene (SPINK1) cause familial or/and hereditary pancreatitis

Le, Maréchal, Chen, JM, Le, Gall, Plessis, G, Chipponi, J, Chuzhanova, NA ORCID: 0000-0002-4655-3618, Raguénès, O and Férec, C, 2004. Two novel severe mutations in the pancreatic secretory trypsin inhibitor gene (SPINK1) cause familial or/and hereditary pancreatitis. Human Mutation (Mutation in Brief) (683).

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Item Type: Journal article
Publication Title: Human Mutation (Mutation in Brief)
Creators: Le, M., Chen, J.M., Le, G., Plessis, G., Chipponi, J., Chuzhanova, N.A., Raguénès, O. and Férec, C.
Date: 2004
Number: 683
Divisions: Schools > School of Science and Technology
Depositing User: EPrints Services
Date Added: 09 Oct 2015 10:34
Last Modified: 09 Jun 2017 13:33
URI: http://irep.ntu.ac.uk/id/eprint/14866

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