Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy
Movement disorders.
2012 Apr ;
27 (4) :
476-9.
Language English Country United States Media print
Document type Case Reports, Journal Article, Research Support, Non-U.S. Gov't
Persistent link
https://www.medvik.cz/link/pmid22488860
PubMed
22488860
DOI
10.1002/mds.24002
Knihovny.cz E-resources
- MeSH
- Arginine genetics MeSH
- Creutzfeldt-Jakob Syndrome genetics pathology MeSH
- Histidine genetics MeSH
- Middle Aged MeSH
- Humans MeSH
- Magnetic Resonance Imaging MeSH
- Mutation genetics MeSH
- DNA Mutational Analysis MeSH
- Prion Proteins MeSH
- Prions genetics MeSH
- Supranuclear Palsy, Progressive physiopathology MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Arginine MeSH
- Histidine MeSH
- Prion Proteins MeSH
- Prions MeSH
- PRNP protein, human MeSH Browser
Comment In
References provided by Crossref.org
Diagnostics (Basel, Switzerland).
2021 Oct 01 ;
11 (10) :
.
[epub] 20211001
