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Researchers perform thousands of mutations to understand amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis (ALS) is a devastating and incurable nervous system disease that affects nerve cells in the brain and spinal cord, causing loss of muscle control and normally death within a few years of diagnosis. In ALS, as in other neurodegenerative diseases, specific protein aggregates have long been recognized as pathological hallmarks, but it is not clear whether they represent the actual cause of the disease. Indeed, alleviating aggregation has repeatedly failed as a therapeutic strategy for treating neurodegenerative diseases such as Alzheimer’s.

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