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

  1. Kishore R. Kumar MBBS, FRACP1,2,
  2. Christine Klein MD1,*

Article first published online: 2 JUL 2012

DOI: 10.1002/mds.25089

Additional Information

How to Cite

Kumar, K. R. and Klein, C. (2012), Commentary for “genetic Creutzfeldt–Jakob disease with R208H mutation presenting as progressive supranuclear palsy”. Mov. Disord.. doi: 10.1002/mds.25089

Author Information

  1. 1

    Section of Clinical and Molecular Neurogenetics at the Department of Neurology, University of Lübeck, Lübeck, Germany

  2. 2

    Department of Neurogenetics, Kolling Institute of Medical Research, Royal North Shore Hospital and University of Sydney, Sydney, New South Wales, Australia

*Department of Neurology, University of Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany

  1. †

    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).

  2. ‡

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

Publication History

  1. Article first published online: 2 JUL 2012
  2. Manuscript Accepted: 24 MAY 2012
  3. Manuscript Revised: 11 MAY 2012
  4. Manuscript Received: 12 FEB 2012

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