CRISPR/Cas9 Technology as an Emerging Tool for Targeting Amyotrophic Lateral Sclerosis (ALS)

Ewa Kruminis-Kaszkiel1, Judyta Juranek2, Wojciech Maksymowicz3

  • 1Department of Pathophysiology, School of Medicine, Collegium Medicum, University of Warmia and Mazury, 10-900 Olsztyn, Poland. ewa.kruminis@uwm.edu.pl.

Summary

The CRISPR/Cas9 genome editing tool offers novel therapeutic strategies for amyotrophic lateral sclerosis (ALS). This review explores its principles, limitations, and applications in modeling and treating ALS, including SOD1-linked and sporadic forms.

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