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Foundation News

A Foundation-funded study found that mutations in the HK1 gene also caused autosomal dominant retinitis pigmentosa in families from Canada and Sicily.
The Foundation is allocating $1.5 million for the development of treatments targeting a variety of retinal diseases.
The Foundation’s co-founder provided financial commentary and discussed the reasons behind The Gordon and Llura Gund Family Challenge.
Advances in AOSLO technology are increasing the likelihood of finding the best candidates.

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