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UW researchers devise approach to treat rare, incurable form of blindness

With many gene therapy options now entering the clinic, which option is best? It depends...on what exact mutation you have. Here's our new case study for one inherited disease featuring #stemcells #crispr #SingleCell

 

We  have developed a gene therapy strategy that may treat a rare, incurable form of blindness known as Best disease. For more go to http://go.wisc.edu/ri2024