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Showing articles 0 to 2 of 2 Filter Applied: methylmalonic aciduria (Click to remove) Hereditary Defect of Cobalamin Metabolism (cblG Mutation) Presenting as a Neurologic Disorder in Adulthood NEJM 318:1738-1741, 1752-17541988., Carmel,R.,et al, 1988 A Young Man with Progressive Subcortical Lesions and Optic Nerve Atrophy Neurol 79:e63, Komatsuzaki, S.,et al, 2012 Showing articles 0 to 2 of 2