A 22-Year-Old Woman with Episodic Weakness and Jaundice
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Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients
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Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes
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Agenesis of the Corpus Callosum:A Marker for Inherited Metabolic Disease
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Agenesis of the Corpus Callosum and Gyral Malformations are Frequent Manifestations of Nonketotic Hyperglycinemia
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