CRISPR/cas9 genome editing techniques are used to replace the endogenous 6 CGG repeat sequence in the 5'; UTR of the gene with a human patient cell line derived 341 CGG repeat sequence. (J:334060)
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CRISPR/cas9 genome editing techniques are used to replace the endogenous 6 CGG repeat sequence in the 5'; UTR of the gene with a human patient cell line derived 341 CGG repeat sequence. (J:334060)