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Glycine encephalopathy
Glycine encephalopathy (GE) is an inborn error of glycine metabolism characterized by accumulation of glycine in body fluids and tissues, including the brain, resulting in neurometabolic symptoms of variable severity.
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Atypical glycine encephalopathy 0 trials
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Glycine encephalopathy 1 0 trials
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Glycine encephalopathy 2 0 trials
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Infantile glycine encephalopathy 0 trials
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Neonatal glycine encephalopathy 0 trials