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Single base substitution protein, and composition comprising same
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Hemophilia b rat model
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Manipulated immune cell
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Genome editing for treating autoimmune disease
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Gene editing of anticoagulants
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Target specific crispr mutant
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Target Specific CRISPR variants
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Method for identifying base editing by using adenosine deaminase
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Composition for treating hemophilia a by crispr/cas system of reverting fviii gene inversion
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Genome editing for treating Retinal dysfunction disease
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Artificial genome manipulation for gene expression regulation
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Target-specific crispr mutant
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Platform for expressing protein of interest in liver
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A system for genome editing toward repeat expansion mutation
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Artificially engineered immune cells
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Pharmaceutical composition for preventing or treating neurological diseases or cardiovascular diseases including stem cells secreting sRAGE
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