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: https://orcid.org/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, 23 (2), p. 205. ISSN 1059-7794

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Item Type:	Journal article
Publication Title:	Human Mutation
Creators:	Le, M., Chen, J.M., Le, G., Plessis, G., Chipponi, J., Chuzhanova, N.A., Raguénès, O. and Férec, C.
Publisher:	John Wiley & Sons
Date:	2004
Volume:	23
Number:	2
ISSN:	1059-7794
Identifiers:	Number Type 10.1002/humu.9212 DOI 498569 Other
Divisions:	Schools > School of Science and Technology
Record created by:	EPrints Services
Date Added:	09 Oct 2015 10:34
Last Modified:	07 May 2024 11:21
URI:	https://irep.ntu.ac.uk/id/eprint/14866

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