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CRISPR Gene Editing Trial Shows Promise In Treating Inherited Blindness

Published: May 6, 2024

A recent clinical trial has shown promising results for a CRISPR/Cas9 gene editing therapy that could potentially restore vision in individuals with a rare type of inherited or congenital blindness.

Source: rttnews.com

Related Topics:

Leber Congenital AmaurosisEric PierceGene Editing TherapyDit 101