Due to a typographical error, the revised date for the above-referenced article was misprinted. The correct revised date is 3 June 2007. Part of the Fig. 4J-L legend appeared incorrectly in the above-referenced article. The entire figure and legend are reprinted here.
Wolfram syndrome 1 (Wfs1) gene expression in the normal mouse visual system
β Scribed by June Kawano; Yukio Tanizawa; Koh Shinoda
- Book ID
- 118283085
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 412 KB
- Volume
- 510
- Category
- Article
- ISSN
- 0021-9967
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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
Wolfram syndrome (WS), a rare autosomal recessive neurodegenerative disorder, results in most cases from mutations in the WFS1 gene. In this study, a total of 19 patients with Wolfram syndrome and 36 relatives from 17 families were screened for mutations in the WFS1 gene. WFS1 mutations were identif