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

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

doi:10.1038/79178

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

Identifier:nobleid.org/w1/20260515/0E40C46F

Type:Journal Article

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

Identifier:nobleid.org/w1/20260515/0E40C46F

Type:Journal Article

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