Commentary for “Genetic Creutzfeldt–Jakob disease with R208H mutation presenting as progressive supranuclear palsy”

Authors

  • Kishore R. Kumar MBBS, FRACP,

    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
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  • Christine Klein MD

    Corresponding author
    1. Section of Clinical and Molecular Neurogenetics at the Department of Neurology, University of Lübeck, Lübeck, Germany
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  • Relevant conflicts of interest/financial disclosures: Kishore R. Kumar receives funding from the Dora Lush NHMRC postgraduate scholarship. Christine Klein is supported by grants from the Volkswagen Foundation (Lichtenberg Grant), the Hermann and Lilly Schilling Foundation, and the BMBF (01GI0201).

  • Full financial disclosures and author roles may be found in the online version of this article.

No abstract is available for this article.

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