<ul><li>Doctors corrected a specific genetic sequence in a patient's genome using CRISPR, making history.</li><li>The drug developed for the patient is specific to his genetic sequence and is unlikely to be used for another person.</li><li>Experts view the approach to help the patient as the future of gene and cell therapies, although it is still in early stages.</li><li>Unlike traditional methods, the treatment directly edited the patient's liver cells in vivo using lipid nanoparticles to deliver the CRISPR components.</li></ul>

CRISPR: Bespoke healthcare

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