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CRISPR extends lifespan of Lou Gehrigs disease mice by 25% – Next Big Future


Next Big Future

CRISPR extends lifespan of Lou Gehrigs disease mice by 25%
Next Big Future
The therapy delayed the onset of the muscle wasting that characterizes the disease, which results in progressive weakness and eventually proves fatal when the muscles that control breathing fail. This step toward a CRISPR cure for human ALS will be
Gene Editing Delays Disease Onset in ALS Model MiceAlzforum



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2017-12-21 NEWS
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