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December 19, 2016Journal of Inherited Metabolic Disease

A SLC39A8 variant causes manganese deficiency, and glycosylation and mitochondrial disorders

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Authors

LRLisa G. RileyMCMark J. CowleyVGVelimir Gayevskiy

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Riley et al. (2016) studied this question.

synapsesocial.com/papers/6aae102fbf071f5ebef83d6bhttps://doi.org/10.1007/s10545-016-0010-6
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