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1:14
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Harvard Medical School
First Patient to Receive a CRISPR Gene-Editing Therapy for Sickle Cell Disease Shares Her Story
Victoria Gray’s life completely changed after she became the first person to receive CRISPR-based gene therapy for sickle cell disease. Sickle cell disease is a painful condition that stems from a mutation in the gene that makes hemoglobin, the protein in red blood cells that carries oxygen throughout the body. Decades of crucial discoveries ...
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