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Showing articles 0 to 2 of 2 Filter Applied: homocystinuria (Click to remove) Analysis of 70 patients with hydrocephalus due to cobalamin C deficiency Neurol 95:e3129-e3137, He, R.,et al, 2020 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 Showing articles 0 to 2 of 2