CRISPR-Cas9 gene-editing tool repairs defective T cells to treat rare hereditary disease – News-Medical.Net
Posted: February 5, 2024 at 2:47 am
CRISPR-Cas9 gene-editing tool repairs defective T cells to treat rare hereditary disease News-Medical.Net
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CRISPR-Cas9 gene-editing tool repairs defective T cells to treat rare hereditary disease - News-Medical.Net
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