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[DOI] [PubMed] [Google Scholar] 102.Israni AK, Xiong H, Liu J, Salkowski N, Trotter JF, Snyder JJ, et al

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Specifically, mutations in SLC39A8, a metal transporter responsible for cellular Mn uptake, associated with Mn deficiency result in cerebral atrophy with subsequent developmental delay, dystonia, and seizures (Riley et al., 2017)