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

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
Depositing User: EPrints Services
Date Added: 09 Oct 2015 10:44
Last Modified: 09 Jun 2017 13:37
URI: http://irep.ntu.ac.uk/id/eprint/17468

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