https://www.biospace.com/article/cber-to-launch-operation-warp-speed-for-rare-diseases-by-year-s-end/
https://www.timesnownews.com/technology-science/6-ways-azure-ai-is-empowering-people-with-disabilities-article-99727313
https://www.express.co.uk/news/science/1659838/blindness-uk-gene-therapy-meiragtx-inherited-eye-disease-shoreditch-london
Publication Date: May 22, 2023
Authors: Dr Sovan Sarkar, Professor Timothy Barrett
Significance
In a study published in Stem Cell Reports the Sarkar and Barrett labs have defined the molecular basis of neurodegeneration in Wolfram Syndrome patients carrying the WFS1 gene mutation.
https://www.ophthalmologytimes.com/view/arvo-live-epigenetic-reprogramming-to-reverse-aging-and-restore-function-to-retinal-ganglion-cells
https://www.express.co.uk/news/science/1659838/blindness-uk-gene-therapy-meiragtx-inherited-eye-disease-shoreditch-london/amp
About the Snow Foundation
The Snow Foundation is a collective voice for Wolfram syndrome patients, working towards a cure for Wolfram syndrome and developing novel therapies for diabetes, vision loss, hearing loss and neurodegeneration.
Rare Diseases…Common Problems
P.O. Box 50224 Clayton, MO 63105
(402) 694-1354
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