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Normalized β‐band power in the sensorimotor network is decreased in amyotrophic lateral sclerosis (ALS) patients and shows correlation with the clinical measures of motor symptom severity (lower motor neuron [LMN] score and fine motor function subscore) and progression. The presented p‐values are after false discovery rate (q = 0.05) correction, and statistical significance is considered as p < 0.05. CON, control; UMN, upper motor neuron.
