Allele-specific silencing of the gain-of-function mutation in Huntington's disease using CRISPR/Cas9.
Shin JW, Hong EP, Park SS, Choi DE, Seong IS, Whittaker MN, Kleinstiver BP, Chen RZ, Lee JM
JCI Insight. 2022 Oct 10;7(19):e141042. doi: 10.1172/jci.insight.141042.
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