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Primary carnitine deficiency is a genetic disorder of the cellular carnitine delivery system that typically manifests around the age of five with symptoms of cardiomyopathy, skeletal muscle weakness and hypoglycemia
Biologically, it is known as the "master antioxidant" because of its ability to recycle other antioxidants, as well as protect cells from oxidative damage
The IGF-1R promoter is targeted by several oncogenes
Can peptide therapy replace traditional hormone replacement completely
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