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PMID 3046314
[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
Reproductive Biomedicine Online, 59 (2), 255267
I wonder what these patients had recorded as cause of death
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