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Intellia, Regeneron ace first trial with ‘in vivo’ CRISPR drug

Phil Taylor ATTR amyloidosis, CRISPR/Cas9, gene editing, Intellia Therapeutics, rare disease, Regeneron 0 Comment

The first ever clinical data with a CRISPR/Cas9 drug used to edit the genomes of cells within the

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Intellia, Regeneron ace first trial with ‘in vivo’ CRISPR drug

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