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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

Genomics 213 ServedioV.dApolitoM.MaioranoN.MinutiB.TorricelliF.RonchiF.et al (2005)

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