Article info
PDFRare disease
CASE REPORT
Rare histotype of sporadic Creutzfeldt-Jakob disease, clinically suspected as corticobasal degeneration
- Correspondence to Mr Bension Shlomo Tilley, bt1112{at}ic.ac.uk
Citation
Rare histotype of sporadic Creutzfeldt-Jakob disease, clinically suspected as corticobasal degeneration
Publication history
- Accepted February 15, 2019
- First published March 7, 2019.
Online issue publication
January 25, 2023
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© BMJ Publishing Group Limited 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/