Engineering miniature CRISPR-Cas Un1Cas12f1 for efficient base editing

Adeno-associated virus (AAV) is a relatively safe and efficient vector for gene therapy. However, due to its 4.7-kb limit of cargo, SpCas9-mediated base editors cannot be packaged into a single AAV vector, which hinders their clinical application. The development of efficient miniature base editors...

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Main Authors: Yueer Hu (Author), Linxiao Han (Author), Qiqin Mo (Author), Zengming Du (Author), Wei Jiang (Author), Xia Wu (Author), Jing Zheng (Author), Xiao Xiao (Author), Yadong Sun (Author), Hanhui Ma (Author)
Format: Book
Published: Elsevier, 2024-06-01T00:00:00Z.
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