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

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Le, M., Chen, J.M., Le, G., Plessis, G., Chipponi, J., Chuzhanova, N.A. 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
Record created by:	EPrints Services
Date Added:	09 Oct 2015 10:34
Last Modified:	09 Jun 2017 13:33
URI:	https://irep.ntu.ac.uk/id/eprint/14866