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Gene Therapy for the Retinal Degeneration of Usher Syndrome Caused by Mutations in MYO7A.
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https://doi.org/10.1101/cshperspect.a017319Abstract
Usher syndrome is a deaf-blindness disorder. One of the subtypes, Usher 1B, is caused by loss of function of the gene encoding the unconventional myosin, MYO7A. A variety of different viral-based delivery approaches have been tested for retinal gene therapy to prevent the blindness of Usher 1B, and a clinical trial based on one of these approaches has begun. This review evaluates the different approaches.
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