Return to site
UW researchers devise approach to treat rare, incurable form of blindness
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 stem cells, CRISPR, and single cell technologies. For more go to http://go.wisc.edu/ri2024