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FDA advisers see no roadblocks for gene-editing treatment for sickle cell disease

FDA advisers see no roadblocks for gene-editing treatment for sickle cell disease
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FDA advisers see no roadblocks for gene-editing treatment for sickle cell disease

FDA advisers see no roadblocks for gene-editing treatment for sickle cell disease
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FDA advisers see no roadblocks for gene-editing treatment for sickle cell disease

FDA advisers see no roadblocks for gene-editing treatment for sickle cell disease
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FDA advisers see no roadblocks for gene-editing treatment for sickle cell disease

FDA advisers see no roadblocks for gene-editing treatment for sickle cell disease
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FDA advisers see no roadblocks for gene-editing treatment for sickle cell disease

Advisers to the Food and Drug Administration meeting Tuesday paved the way for the first treatment of human disease using the gene-editing technique CRISPR. The agency has a December deadline.

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