Commentary for "Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy"

Mov Disord. 2014 Jun;29(7):E1-2. doi: 10.1002/mds.25089. Epub 2012 Jul 2.

Authors

Kishore R Kumar¹, Christine Klein

Affiliation

¹ Section of Clinical and Molecular Neurogenetics at the Department of Neurology, University of Lübeck, Lübeck, Germany; Department of Neurogenetics, Kolling Institute of Medical Research, Royal North Shore Hospital and University of Sydney, Sydney, New South Wales, Australia.

PMID: 22753322
DOI: 10.1002/mds.25089

No abstract available

Publication types

Research Support, Non-U.S. Gov't
Comment

MeSH terms

Arginine / genetics*
Creutzfeldt-Jakob Syndrome / genetics*
Female
Humans
Mutation / genetics*
Prions / genetics*
Supranuclear Palsy, Progressive / physiopathology*

Substances

Prions
Arginine