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Biomaterials as vectors for the delivery of CRISPR–Cas9 Joon Eoha and Luo Gu*a The emergence of the CRISPR–Cas9 gene editing system has brought much hope and excitement to the field of gene therapy and the larger scientific community. However, in order for CRISPR-based therapies to be translated to the clinical setting, there is an urgent need to develop optimized vectors for their delivery.
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