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        Retrovirus-Mediated Gene Transfer to Human Hematopoietic Stem Cells

        互联网

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        The ability of hematopoietic stem cells (HSCs) to engraft in a recipient and establish long-term repopulation of the hematopoietic system makes them ideal targets for gene therapy vectors designed to correct inherited or acquired diseases affecting the hematopoietic and immune systems.
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