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Mashup Score: 4News: Genome Editing With Cas9 and AAV Generates Frequent Insertion of Viral Vectors That Are Difficult to Detect - CRISPR Medicine - 17 day(s) ago
Researchers in the US, Japan and the UK report in Nature Biotechnology that genome editing with Cas9 and adeno-associated virus repair templates leads to frequent insertion of viral vectors that are difficult to detect.
Source: crisprmedicinenews.comCategories: General Medicine News, Future of MedicineTweet
Genome editing with Cas9 and AAV generates frequent insertion of viral vectors that are difficult to detect #NBTintheNews https://t.co/lgbDKL62SW