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mmunity of researchers that are interested in timecourse of motor training.(1) Background Molybdenum cofactor deficiency type B (MOCODB, #25216 is a rare autosomal recessive metabolic disorder characterized by intractable seizures of neonatal-onset, muscular spasticity, accompanying with hypouricemia, elevated urinary sulfite levels and craniofacial dysmorphism. Thirty-five patients were reported to date. (2) Methods Our paper aimed to delineate the disease genotype by presenting another patient, in whom a novel, in-frame variant with

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