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European Journal of Medical Genetics|October 12, 2010
Parental origin and functional relevance of a de novo UBE3A variantBernhard Horsthemke, Michaela Wawrzik, Stephanie Gross, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 14, 2017
Movement disorders in genetically confirmed mitochondrial disease and the putative role of the cerebellumSebastian R Schreglmann, Franz Riederer, Marian Galovic, et al.Pageof 1