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24. Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a family. Wei W; Zheng XF; Ruan DD; Gan YM; Zhang YP; Chen Y; Lin XF; Tang FQ; Luo JW; Li YF Neurol Sci; 2022 Apr; 43(4):2555-2563. PubMed ID: 34783933 [TBL] [Abstract][Full Text] [Related]
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