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[99] A person with cobalamin C disease, a rare autosomal, recessive, inheritance disease which results in combined methylmalonic aciduria and homocystinuria), [100] can be treated with intravenous or intramuscular hydroxocobalamin

M., Sun, J., Sharma, L., Libinaka, R., Jiang, W

Mild mood changes tied to deficiency often start shifting here too

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