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Description
Skeletal-muscle metabolic reprogramming in ALS-SOD1G93A mice predates disease onset and is a promising therapeutic target
Primary carnitine deficiency is a genetic disorder of the cellular carnitine-transporter system that typically appears by the age of five with symptoms of cardiomyopathy, skeletal-muscle weakness, and hypoglycemia
Erythrocyte superoxide dismutase as a biomarker of septic acute kidney injury
doi: 10.1152/jappl.1986.61.4.1275
