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A voice for rare disease, working towards a cure for Wolfram syndrome and developing novel therapies for diabetes, vision loss, hearing loss neurodegeneration. Raising awareness and funding for Wolfram Syndrome research, an ultra rare disease. 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.
455308117
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2012
Founded
Clayton, MO 63105 USA
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thesnowfoundation.org
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Find Your Community Rare Diseases Common Problems NeverLose Hope Learn Learn more about Wolfram Syndrome. Donate Find out ways you can donate. Events Check out our upcoming events. Community Engage with your extended Wolfram family.

Specifically Named Diseases Research Specifically Named Diseases Health - General & Rehabilitative N.E.C.
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