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S.ArmstrongC
SLC22A5 mutations impair OCTN2 function, causing primary carnitine deficiency (PCD) (1517), an autosomal recessive disorder characterized by skeletal myopathy, progressive cardiomyopathy, hypoglycemia, and hyperammonemia
Skin autofluorescence as a potential adjunctive marker for cardiovascular risk assessment in type 2 diabetes: a systematic review
Gut infections can impact nutrient absorption, metabolism, mitochondrial health, and the immune system
