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Using CRISPR To Cure Childhood Blindness

April 1, 2021

A person with Leber’s has become the first to receive a CRISPR–Cas9 gene therapy administered directly into their body. The treatment is part of a landmark clinical trial named ‘BRILLIANCE’, which tests the ability of CRISPR–Cas9 gene-editing techniques to remove the mutations that cause the rare genetic condition.

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