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Office of Dietary Supplements NIoH
Less severe SLC22A5 mutations can cause skeletal muscle problems or cardiomyopathy
As a result, the antioxidant hypothesis ASD remains supported largely by preclinical evidence and by indirect clinical observations rather than by robust biochemical validation in patients
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doi:10.1519/JSC.0000000000001223 Mabrey, G., Koozehchian, M
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