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The disease is caused by a mutation in the ATP7B gene, which codes for a protein that facilitates the incorporation of copper into proteins (such as ceruloplasmin) and also the transportation of copper into vesicles that allow it to be secreted in bile.1 The critical effect of a mutation in ATP7B is diminished copper secretion into bile, which leads to excess copper accumulation in the hepatocyte

On the other hand, if you have a particularly long or thick beard, you might need a bit more

Then, the TCA cycle is operating to produce reducing compounds to maintain cellular redox balance 38

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Theres no recommended upper limit for B12, so overdosing is not a concern