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A single base-pair deletion in the WFS1 gene causes Wolfram syndrome

✍ Scribed by Pitt, Katherine; James, Chela; Kochar, Inderpal S.; Kapoor, Akshay; Jain, Shilpi; Hussain, Khalid; Bennett, Kate

Book ID
121455602
Publisher
Walter de Gruyter GmbH & Co. KG
Year
2011
Tongue
English
Weight
144 KB
Volume
24
Category
Article
ISSN
0334-018X

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## Abstract Confocal laser scanning microscope image of double immunostaining for Wfs1 protein (green) and for glial fibrillary acidic protein (GFAP; an astrocyte marker; red) in the normal mouse retina and optic nerve. Cell nuclei are labeled in blue. The Wfs1 protein, also called wolframin, is th