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The Human Protein Atlas
[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
The FUT2 secretor variant worsens B12 status in cases with heterozygous gastric intrinsic factor mutations by impairing gastric intrinsic factor secretion (56)
The definition of vitamin B 12 (cobalamin) deficiency varies with the assay used
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