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Nourshahi, M., Kaviani, M., Kimiagar, M., and Ebrahim, K

If the forearm ischemic test result is abnormal (in line with glycolysis pathway enzymatic deficiencies), then genetic testing for McArdles disease is in order as the latter is the most common glycolytic pathway enzyme deficiency

and (3) In any cases, not all patients with ASD have altered levels of carnitine

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