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CRISPR-Cas9-AAV versus lentivector transduction for genome modification of X-linked severe combined immunodeficiency hematopoietic stem cells.
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Multiplex HDR for disease and correction modeling of SCID by CRISPR genome editing in human HSPCs.
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Genomic Engineering in Human Hematopoietic Stem Cells: Hype or Hope?
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Advances and Obstacles in Homology-Mediated Gene Editing of Hematopoietic Stem Cells.
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