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New, modified CRISPR protein can fit inside virus used for gene therapy - EurekAlert
Researchers have developed a novel version of a key CRISPR gene-editing protein that shows efficient editing activity and is small enough to be packaged within a non-pathogenic virus that can deliver it to target cells. Hongjian Wang and colleagues at Wuhan University, China, present these findings May 23rd in the open-access journal PLOS Biology.
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