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This review discusses the potential of CRISPR technology as an alternative approach to treat neurodegenerative diseases (NDs), which currently lack effective disease-modifying therapies. It highlights how CRISPR can enable precise genetic modifications to target the underlying causes of NDs, contrasting with existing treatments that primarily focus on symptom management. The review also addresses the challenges and ethical implications of implementing CRISPR-based therapies while providing a comprehensive a

Author

aleena

Language

EN