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Hereditary Disorders of Manganese Metabolism: Pathophysiology of Childhood-Onset Dystonia-Parkinsonism in SLC39A14 Mutation Carriers and Genetic Animal Models.
Int J Mol Sci. 2022 Oct 24;23(21):12833. doi: 10.3390/ijms232112833.
Int J Mol Sci. 2022.
PMID: 36361624
Free PMC article.
Review.
Behavioral and neurochemical studies of inherited manganese-induced dystonia-parkinsonism in Slc39a14-knockout mice.
Rodichkin AN, Edler MK, McGlothan JL, Guilarte TR.
Rodichkin AN, et al.
Neurobiol Dis. 2021 Oct;158:105467. doi: 10.1016/j.nbd.2021.105467. Epub 2021 Aug 4.
Neurobiol Dis. 2021.
PMID: 34358615
Free PMC article.
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Pathophysiological studies of aging Slc39a14 knockout mice to assess the progression of manganese-induced dystonia-parkinsonism.
Rodichkin AN, Edler MK, McGlothan JL, Guilarte TR.
Rodichkin AN, et al.
Neurotoxicology. 2022 Dec;93:92-102. doi: 10.1016/j.neuro.2022.09.005. Epub 2022 Sep 22.
Neurotoxicology. 2022.
PMID: 36152728
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