Referenced in: none

Automatically associated channels: Kir1.1 , Kir6.2

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

Authors: M Bitner-Glindzicz, 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

Journal, date & volume: Nat. Genet., 2000 Sep , 26, 56-60

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/10973248

Abstract