Gene editing for HD: Therapeutic prospects
Author:
Publisher
Elsevier
Reference116 articles.
1. RNA targeting with CRISPR–Cas13;Abudayyeh;Nature,2017
2. Predicting the mutations generated by repair of Cas9-induced double-strand breaks;Allen;Nature Biotechnology,2019
3. Structure and expression of the Huntington's disease gene: Evidence against simple inactivation due to an expanded CAG repeat;Ambrose;Somatic Cell and Molecular Genetics,1994
4. Development of TTX-3360 to treat/prevent HD and other repeat expansion disorders by halting somatic expansion;Antonijevic,2021
5. Programmable deletion, replacement, integration and inversion of large DNA sequences with twin prime editing;Anzalone;Nature Biotechnology,2022
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