Coinheritance of a novel deletion of the entire SPINK1 gene with a CFTR missense mutation (L997F) in a family with chronic pancreatitis

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Masson, E., Le, M., Levy, P., Chuzhanova, N. ORCID: 0000-0002-4655-3618, Cooper, D.N., Chen, J.M. and Férec, C., 2007. Coinheritance of a novel deletion of the entire SPINK1 gene with a CFTR missense mutation (L997F) in a family with chronic pancreatitis. Molecular Genetics and Metabolism, 92, pp. 168-175.

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Item Type:	Journal article
Publication Title:	Molecular Genetics and Metabolism
Creators:	Masson, E., Le, M., Levy, P., Chuzhanova, N., Cooper, D.N., Chen, J.M. and Férec, C.
Date:	2007
Volume:	92
Divisions:	Schools > School of Science and Technology
Record created by:	EPrints Services
Date Added:	09 Oct 2015 10:44
Last Modified:	09 Jun 2017 13:37
URI:	https://irep.ntu.ac.uk/id/eprint/17468