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Gene-Editing Therapy Helps Nashville Sickle Cell Patients | City Limits

In early December, CRISPR-Cas9 gene editing therapy was approved by the Food and Drug Administration for the treatment of sickle cell in patients ages 12 and up. It’s the first FDA approval for the gene-editing therapy, whose creators won the Nobel Prize in chemistry in 2020. ....

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Groundbreaking gene editing therapy helps local sickle cell patients

TriStar Centennial doctor led national CRISPR clinical trial ....

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