Genome editing-mediated knock-in of therapeutic genes ameliorates the disease phenotype in a model of hemophilia
Recently, clinical trials of adeno-associated virus-mediated replacement therapy have suggested long-term therapeutic effects for several genetic diseases of the liver, including hemophilia. However, there remain concerns regarding decreased therapeutic effects when the liver is regenerated or when...
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Elsevier,
2022-09-01T00:00:00Z.
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Internet
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A1234.567 |
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