Hereditary Defect of Cobalamin Metabolism (cblG Mutation) Presenting as a Neurologic Disorder in Adulthood
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Mendelian Etiologies of Stroke
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A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
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A Young Woman with Rapid Mental Deterioration and Leukoencephalopathy
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Homocystinuria Due to 5, 10-Methylenetetrahydrofolate Reductase Deficiency Revealed by Stroke in Adult Siblings
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