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Another research discrepancy was found in the study done by Yoon HS., et al
110(4): 2869 Naisbitt DJ, Hough SJ, Gill HJ, et al
154,155,156,157 Currently, the CRISPR/Cas9 system can enter cells for gene editing in three forms: the Cas9: sgRNA ribonucleoprotein complex, mRNA for Cas9 translation alongside a separate sgRNA, and a DNA plasmid that encodes both the Cas9 protein and sgRNA
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