CRISPR/Cas9-mediated gene editing ameliorates neurotoxicity in mouse model of Huntington’s disease
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Link
https://www.jci.org/articles/view/92087/files/pdf
Reference21 articles.
1. Huntington disease;Bates;Nat Rev Dis Primers,2015
2. Potent and Selective Antisense Oligonucleotides Targeting Single-Nucleotide Polymorphisms in the Huntington Disease Gene / Allele-Specific Silencing of Mutant Huntingtin
3. Allele-Specific Silencing of Mutant Huntingtin in Rodent Brain and Human Stem Cells
4. CRISPR/Cas9 Editing of the Mutant Huntingtin Allele In Vitro and In Vivo
5. RNA interference improves motor and neuropathological abnormalities in a Huntington's disease mouse model
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