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  • CRISPR-Cas9 has been used in mice to disable a defective gene that causes amyotrophic lateral sclerosis. Treated mice had 50% more motor neurons at end stage, experienced a 37% delay in disease onset,

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CRISPR-Cas9 has been used in mice to disable a defective gene that causes amyotrophic lateral sclerosis. Treated mice had 50% more motor neurons at end stage, experienced a 37% delay in disease onset,

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