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

Le, M., Chen, J.M., Le, G., Plessis, G., Chipponi, J., Chuzhanova, N.A. ORCID: 0000-0002-4655-3618, Raguénès, O. and Férec, C., 2003. Two novel severe mutations in the pancreatic secretory trypsin inhibitor gene (SPINK1) cause familial or/and hereditary pancreatitis. American Journal of Human Genetics, 73 (5), p. 565.

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Item Type: Journal article
Publication Title: American Journal of Human Genetics
Creators: Le, M., Chen, J.M., Le, G., Plessis, G., Chipponi, J., Chuzhanova, N.A., Raguénès, O. and Férec, C.
Date: 2003
Volume: 73
Number: 5
Divisions: Schools > School of Science and Technology
Record created by: EPrints Services
Date Added: 09 Oct 2015 10:39
Last Modified: 09 Jun 2017 13:35
URI: https://irep.ntu.ac.uk/id/eprint/16112

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