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6d) have been used to identify the core phenotype of Mn deficiency, which includes glycosylation defects (resembling type II CDG), mitochondrial dysfunction, intellectual disability, growth retardation, and cerebral atrophy 209,214,215,217

Int J Emerg Med

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We observed that incubation of proteins with a C-terminal MESNA thioester with glutathione results in the formation of an unstable C-terminal glutathione-thioester, followed by hydrolysis to a carboxyl group

doi: 10.1111/1541-4337.12755 82

Severe hypokalaemia (low blood potassium) is rare but can develop in some cases, particularly in severe megaloblastic anaemia or in patients taking certain medications such as diuretics