UF researchers develop gene therapy that could correct a common form of blindness

Monday, January 23, 2012

A new gene therapy method developed by University of Florida researchers has the potential to treat a common form of blindness that strikes both youngsters and adults. The technique works by replacing a malfunctioning gene in the eye with a normal working copy that supplies a protein necessary for light-sensitive cells in the eye to function. The findings are published today in the Proceedings of the National Academy of Sciences online.

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