Publication Name	World Journal of Clinical Cases
Manuscript ID	85937
Country	China

Received	2023-05-26 13:06
Peer-Review Started	2023-05-26 13:12
To Make the First Decision
Return for Revision	2023-07-17 09:13
Revised	2023-07-25 08:06
Second Decision	2023-08-09 02:57
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2023-08-09 08:24
Articles in Press	2023-08-09 08:24
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2023-08-23 06:46
Publish the Manuscript Online	2023-09-01 09:10

ISSN	2307-8960 (online)
Open Access	This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (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: https://creativecommons.org/Licenses/by-nc/4.0/
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Category	Clinical Neurology
Manuscript Type	Case Report
Article Title	Creutzfeldt-Jakob disease presenting as Korsakoff syndrome caused by E196A mutation in PRNP gene: A case report
Manuscript Source	Unsolicited Manuscript
All Author List	Yong-Kang Zhang, Jia-Rui Liu, Kang-Li Yin, Yuan Zong, Yu-Zhen Wang and Ye-Min Cao
ORCID	Author(s) ORCID Number Yong-Kang Zhang http://orcid.org/0000-0002-2156-6762 Ye-Min Cao http://orcid.org/0000-0001-5961-1058
Funding Agency and Grant Number
Corresponding Author	Ye-Min Cao, Doctor, MD, PhD, Academic Research, Chief Doctor, Professor, Shanghai TCM-Integrated Hospital, Shanghai University of Traditional Chinese Medicine, Diagnosis and Treatment Center of Vascular Disease, No. 230 Road Baoding, Hongkou District, Shanghai 200082, China. caoyemin@shutcm.edu.cn
Key Words	Prion disease; Creutzfeldt-Jakob disease; Korsakoff syndrome; PRNP gene; 14-3-3 proteins; Case report
Core Tip	The present case report describes a rare mutation in the prion protein gene at codon 196 causing Creutzfeldt-Jakob disease (CJD) with a clinical presentation of Korsakoff syndrome. This study emphasizes the importance of considering this mutation in CJD patients presenting with Korsakoff syndrome based on clinical, laboratory, and imaging findings.
Publish Date	2023-09-01 09:10
Citation	Zhang YK, Liu JR, Yin KL, Zong Y, Wang YZ, Cao YM. Creutzfeldt-Jakob disease presenting as Korsakoff syndrome caused by E196A mutation in PRNP gene: A case report. World J Clin Cases 2023; 11(25): 5982-5987
URL	https://www.wjgnet.com/2307-8960/full/v11/i25/5982.htm
DOI	https://dx.doi.org/10.12998/wjcc.v11.i25.5982

Full Article (PDF)	WJCC-11-5982-with-cover.pdf
Full Article (Word)	WJCC-11-5982.docx
Manuscript File	85937_Auto_Edited-JLW.docx
Answering Reviewers	85937-Answering reviewers.pdf
Audio Core Tip	85937-Audio core tip.m4a
Conflict-of-Interest Disclosure Form	85937-Conflict-of-interest statement.pdf
Copyright License Agreement	85937-Copyright license agreement.pdf
Signed Consent for Treatment Form(s) or Document(s)	85937-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	85937-Language certificate.pdf
Peer-review Report	85937-Peer-review(s).pdf
Scientific Misconduct Check	85937-Bing-Fan JR-2.png
Scientific Editor Work List	85937-Scientific editor work list.pdf