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1. Introduction Amyotrophic lateral sclerosis (ALS) is a fatal progressive neurodegenerative disease which results in damaging the motor neurons in the brain and spinal cord [1]. Damage to motor neurons leads to atrophy of muscle, diminished strength, and death of the affected patients. About 90% of ALS cases are spontaneous, while 10% are associated with mutations in genes of a dominant trait [2].
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