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Published in 2021 at "Experimental Neurology"
DOI: 10.1016/j.expneurol.2021.113620
Abstract: Amyotrophic lateral sclerosis (ALS) is a devastating, rapidly progressive, neurodegenerative disorder affecting upper and lower motor neurons. Approximately 10% of patients suffer from familial ALS (FALS) with mutations in different ubiquitously expressed genes including SOD1,…
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Keywords:
impairment mitochondrial;
sals fals;
mitochondrial oxidative;
oxidative phosphorylation ... See more keywords