JAG1 mutations are found in approximately one third of patients presenting with only one or two clinical features of Alagille syndrome.

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Published in Clin Genet on July 31, 2011

Authors

K Guegan1, K Stals, M Day, P Turnpenny, S Ellard

Author Affiliations

1: Department of Molecular Genetics Department of Clinical Genetics, Royal Devon & Exeter NHS Foundation Trust, Barrack Road, Exeter, UK. Katie.guegan@rdeft.nhs.uk

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