A glance at what’s happening in the world of technology.
Gene therapy study offers hope to IRD sufferers
The visual function of mice suffering from inherited retinal disease (IRD) was restored in a US study hailed as a breakthrough.
Researchers from the University of California, Irvine (UCI), used new-generation CRISPR technology – known as base editing – to demonstrate a new therapeutic modality for a wide range of IRDs.
Co-author Krzysztof Palczewski, professor at the UCI’s Gavin Herbert Eye Institute, said: “We provide evidence of the clinical potential of base editors for the correction of mutations causing IRDs and for restoring visual function.
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