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In a D-Asp oxidase knockout mouse model, treatment with D-Asp significantly alleviated phencyclidine-induced cortico-limbic thalamic dysfunction and reduced neuronal prepulse deficits induced by psychotropic drugs (amphetamine and MK-801)

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Individuals with autosomal dominant FHI-KATP tend to be appropriate for gestational age at birth, to present at approximately age one year (range: 2 days - 30 years), and to respond to diet and diazoxide therapy