Hereditary Disorders of Manganese Metabolism: Pathophysiology of Childhood-Onset Dystonia-Parkinsonism in <i>SLC39A14</i> Mutation Carriers and Genetic Animal Models.

Int J Mol Sci · 2022 · PMC9653914 · PMID 36361624

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closest p

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The sentences

highly significantno p-value reported

They found highly significant deficits in all motor function tests in the Slc39a14 -KO mice relative to WT.

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