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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

It also helps in the regeneration of glutathione, an enzyme that rids the body of free radicals

In August 2013, the agency required new updates to the labels to describe the potential for irreversible peripheral neuropathy

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They are strictly intended for laboratory research and in vitro experimentation

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