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Secondary mitochondrial dysfunction Multiple Acyl-CoA Dehydrogenase Deficiency (OMIM# 231680) Multiple acyl-coenzyme A dehydrogenase deficiency, also known as glutaric aciduria Type II (GAII), is an autosomal recessive disorder that affects the oxidation of fatty acids, BCAA, lysine, tryptophan, and choline

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Gaze-Following Activities: Teaching children to follow someones eyes to understand attention

75 (Suppl 1), S33S34 (2014)