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).
Article first published online: 2 JUL 2012
Copyright © 2012 Movement Disorder Society
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
Full financial disclosures and author roles may be found in the online version of this article.
- Article first published online: 2 JUL 2012
- Manuscript Accepted: 24 MAY 2012
- Manuscript Revised: 11 MAY 2012
- Manuscript Received: 12 FEB 2012