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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

concerns regarding unpredictable absorption The mechanism for the oral route is based on passive absorption of vitamin B 12 (without binding to intrinsic factor) as well as active absorption (following binding to intrinsic factor, if present, e.g

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