The Ashkenazi Jewish Variant, By Toko Campbell
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
The Snow Foundation is proud to be a PLATINUM MEMBER of The National Organization of Rare Disorders. Check out their Website: https://rarediseases.org/
Wolfram Syndrome Poster Presentation by Brianna Carman-Washington University School of Medicine-Urano Lab
https://medicalxpress.com/news/2023-03-febrile-urinary-tract-infections-common.html
Wolfram Syndrome Poster Presentation by William An and Megha Verma-Washington University School of Medicine-Urano Lab
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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