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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
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Metabolomics 8 (2), 201210
[DOI] [PubMed] [Google Scholar] 69.Hanahan D., Weinberg R.A
10.1080/15548627.2017.1359449 Autophagy 32 HeoJ
