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This article reports a 21-year-old patient with a rare inborn error in homocysteine (HCY) metabolism, severe HHCY due to late-onset MTHFR deficiency which is a novel mutant strain, predominantly presented with neuropsychiatric disorders, whose biochemical abnormalities and clinical symptoms improved in the short term after betaine treatment

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Rapid induction of neurotrophin mRNAs in rat glial cell cultures by Semax, an adrenocorticotropic hormone analog