A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene.

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Published in Nat Genet on September 01, 2000

Authors

M Bitner-Glindzicz1, K J Lindley, P Rutland, D Blaydon, V V Smith, P J Milla, K Hussain, J Furth-Lavi, K E Cosgrove, R M Shepherd, P D Barnes, R E O'Brien, P A Farndon, J Sowden, X Z Liu, M J Scanlan, S Malcolm, M J Dunne, A Aynsley-Green, B Glaser

Author Affiliations

1: Department of Clinical and Molecular Genetics, Institute of Child Health, and Great Ormond Street Hospital for Children NHS Trust, London, UK. mbitnerg@ich.ucl.ac.uk

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