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In vivo CRISPR base editing for treatment of Huntington’s disease

July 29, 2026
in Medicine
Reading Time: 1 min read
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In vivo CRISPR base editing for treatment of Huntington’s disease

In vivo CRISPR base editing for treatment of Huntington’s disease

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Shirguppe, S., Gapinske, M., Swami, D. et al. In vivo CRISPR base editing for treatment of Huntington’s disease.
Nat. Biomed. Eng (2026). https://doi.org/10.1038/s41551-026-01747-y

https://doi.org/10.1038/s41551-026-01747-y

Tags: advancements in neurogenetic therapiesbiomedical engineering in neurogeneticsCRISPR technology in Huntington’s diseaseCRISPR-based gene correction in vivogene editing in neurodegenerative disordersgenome editing for hereditary neurological disordersHuntington’s disease genetic mutation targetingin vivo CRISPR base editing for Huntington’s disease treatmentin vivo gene therapy strategiesmolecular mechanisms of Huntington’s diseasetargeted genetic therapy for Huntington’stherapeutic potential of CRISPR in neurodegeneration
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