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Precise CAG repeat contraction in a Huntington's Disease mouse model is enabled by gene editing with SpCas9-NG.
Oura S, Noda T, Morimura N, Hitoshi S, Nishimasu H, Nagai Y, Nureki O, Ikawa M
Commun Biol. 2021 Jun 23;4(1):771. doi: 10.1038/s42003-021-02304-w.
PubMed Article

Plasmids from Article

ID Plasmid Purpose
171370pX459-SpCas9-NGSpCas9-NG-mediated genome editing.

Antibodies from Article