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International journal of developmental neuroscience: the official journal of the International Society for Developmental Neuroscience.May 2015;42:37-45

Hyperammonemic encephalopathy, sometimes fatal, has been reported following initiation of valproate therapy in patients with urea cycle disorders, a group of uncommon genetic abnormalities, particularly ornithine transcarbamylase deficiency

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De bescherming van cellen tegen oxidatieve stress

Genetic variations in the MUT gene lead to the absence of methylmalonyl CoA mutase, resulting in a blockage of the propionate metabolic pathway