A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene by Bitner-Glindzicz M, Lindley K J, Rutland P, Blaydon D, Smith V V, Milla P J, Hussain K, Furth-Lavi J, Cosgrove K E, Shepherd R M, Barnes P D, O'Brien R E, Farndon P A, Sowden J, Liu X Z, Scanlan M J, Malcolm S, Dunne M J, Aynsley-Green A, Glaser B in Nature genetics (2000).

[PMID: 10973248] PubMed


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