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. ISSN 0002-9297

Full text not available from this repository.

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.
Publisher:	Cell Press
Date:	2003
Volume:	73
Number:	5
ISSN:	0002-9297
Identifiers:	Number Type 507831 Other
Divisions:	Schools > School of Science and Technology
Record created by:	EPrints Services
Date Added:	09 Oct 2015 10:39
Last Modified:	07 May 2024 11:33
URI:	https://irep.ntu.ac.uk/id/eprint/16112

Actions (login required)

Edit View

Views

Downloads