CRISPR 2.0, the Next Generation
51:13
YouTubeThe Aspen Institute
CRISPR 2.0, the Next Generation
History was made this year when the first FDA-approved CRISPR-based gene editing therapy became available to patients, designed to cure sickle cell anemia. That represents ground-breaking progress, but the treatment involves a months-long ordeal with often-brutal side effects and it is hugely expensive. With dozens of CRISPR therapeutics in the ...
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