Publication Name	World Journal of Clinical Cases
Manuscript ID	76671
Country	China

Received	2022-03-25 06:51
Peer-Review Started	2022-03-25 06:53
To Make the First Decision
Return for Revision	2022-06-27 08:08
Revised	2022-07-02 05:51
Second Decision	2022-07-18 03:01
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2022-07-22 02:02
Articles in Press	2022-07-22 02:02
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2022-07-29 08:59
Publish the Manuscript Online	2022-08-16 01:35

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: http://creativecommons.org/Licenses/by-nc/4.0/
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Category	Genetics & Heredity
Manuscript Type	Case Report
Article Title	VARS2 gene mutation leading to overall developmental delay in a child with epilepsy: A case report
Manuscript Source	Unsolicited Manuscript
All Author List	Xiao-Hui Wu, Shuang-Zhu Lin, Yan-Qiu Zhou, Wan-Qi Wang, Jia-Yi Li and Qian-Dui Chen
ORCID	Author(s) ORCID Number Xiao-Hui Wu http://orcid.org/0000-0003-3961-0730 Shuang-Zhu Lin http://orcid.org/0000-0001-5333-2138 Yan-Qiu Zhou http://orcid.org/0000-0001-6834-1723 Wan-Qi Wang http://orcid.org/0000-0002-8247-7616 Jia-Yi Li http://orcid.org/0000-0002-7729-4479 Qian-Dui Chen http://orcid.org/0000-0002-8593-4077
Funding Agency and Grant Number
Corresponding Author	Shuang-Zhu Lin, MD, Doctor, Diagnosis and Treatment Center for Children , The Affiliated Hospital of Changchun University of Chinese Medicine, No. 1478 Gongnong Road, Chaoyang District, Changchun 130103, Jilin Province, China. 61858@163.com
Key Words	Mitochondrial aminoacyl-tRNA synthetase; Mitochondrial diseases; VARS2; Case report
Core Tip	The clinical manifestation of the child was remarkable. Through the comprehensive analysis of symptoms, physical examination, biochemical examination and gene sequencing, the child was confirmed to have combined oxidative phosphorylation deficiency type 20, and the phenotypic spectrum of the disease was thus expanded.
Publish Date	2022-08-16 01:35
Citation	Wu XH, Lin SZ, Zhou YQ, Wang WQ, Li JY, Chen QD. VARS2 gene mutation leading to overall developmental delay in a child with epilepsy: A case report. World J Clin Cases 2022; 10(24): 8749-8754
URL	https://www.wjgnet.com/2307-8960/full/v10/i24/8749.htm
DOI	https://dx.doi.org/10.12998/wjcc.v10.i24.8749

Full Article (PDF)	WJCC-10-8749.pdf
Full Article (Word)	WJCC-10-8749.docx
CARE Checklist–2016	76671-CARE-Checklist–2016-revision.pdf
Manuscript File	76671_Auto_Edited-LS.docx
Answering Reviewers	76671-Answering reviewers.pdf
Audio Core Tip	76671-Audio core tip.mp3
Conflict-of-Interest Disclosure Form	76671-Conflict-of-interest statement.pdf
Copyright License Agreement	76671-Copyright license agreement.pdf
Signed Consent for Treatment Form(s) or Document(s)	76671-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	76671-Language certificate.pdf
Peer-review Report	76671-Peer-review(s).pdf
Scientific Editor Work List	76671-Scientific editor work list.pdf