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Description
Epilepsy and movement disorders: A severe deficiency caused by rare mutations in the PNPO enzyme can result in encephalopathy, epilepsy, and movement disorders from infancy
OS plays a primary role in the pathogenesis of DM (125, 126) as manifested through many enzymatic, non-enzymatic, and mitochondrial mechanisms (127)
Arab J Urol (2018) 16(1):11324
The absorbance values of ABTS+ at 738 nm were recorded to quantify the free radical scavenging ability of MML-CDs
