What it is
In this study, we evaluated the DNA repair outcomes of DNA nicks and mismatches introduced using base editors in human embryos at two targets, PCSK9 and HBG. Editing was efficient and, unlike Cas9-induced DSBs, did not result in either chromosomal abnormalities or large deletions.
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Filed underCRISPR and Genetic Engineering, RNA regulation and disease, Animal Genetics and Reproduction