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