The decision by an advisory committee may lead to Food and Drug Administration approval of the first treatment for humans that uses the CRISPR gene-editing system.
https://siii-clinical.com/wp-content/uploads/2021/09/Untitled-1.png00https://siii-clinical.com/wp-content/uploads/2021/09/Untitled-1.png2023-10-31 22:14:282023-10-31 22:14:28Panel Tells F.D.A. That CRISPR Sickle Cell Cure Is Safe Enough for Patients
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