Precise detection of CRISPR-Cas9 editing in hair cells in the treatment of autosomal dominant hearing loss
Gene therapy would benefit from the effective editing of targeted cells with CRISPR-Cas9 tools. However, it is difficult to precisely assess the editing performance in vivo because the tissues contain many non-targeted cells, which is one of the major barriers to clinical translation. Here, in the A...
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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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Nide 1 | Saatavissa |