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23. Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only. Wilcox R; Brænne I; Brüggemann N; Winkler S; Wiegers K; Bertram L; Anderson T; Lohmann K J Neurol; 2015 Jan; 262(1):187-93. PubMed ID: 25359261 [TBL] [Abstract][Full Text] [Related]
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