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In contrast to low ceruloplasmin levels observed in Wilson disease, the very rare genetic disorder of aceruloplasminemia presents with a more severe neurodegenerative phenotype including ataxia, unvoluntary movements, dystonia, tremor and chorea (34)

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Based on the close similarity of the NO-assays in other tissues (e.g

Gaus K, 2016, 'Erratum: Functional role of T-cell receptor nanoclusters in signal initiation and antigen discrimination (National Academy of Sciences (2016) 113:37 (E5454-E5463) DOI: 10.1073/pnas.1607436113)', Proceedings of the National Academy of Sciences of the United States of America , 113, pp

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