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Commentary for “Genetic Creutzfeldt–Jakob disease with R208H mutation presenting as progressive supranuclear palsy”
Authors:Kishore R. Kumar MBBS  FRACP  Christine Klein MD
Affiliation:1. Section of Clinical and Molecular Neurogenetics at the Department of Neurology, University of Lübeck, , Lübeck, Germany;2. Department of Neurogenetics, Kolling Institute of Medical Research, Royal North Shore Hospital and University of Sydney, , Sydney, New South Wales, Australia
Abstract:
Keywords:
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