Publication Name	World Journal of Clinical Cases
Manuscript ID	43213
Country	China

Received	2018-11-20 02:31
Peer-Review Started	2018-11-20 08:24
To Make the First Decision	2018-12-26 02:49
Return for Revision	2019-01-03 01:15
Revised	2019-01-16 12:34
Second Decision	2019-01-29 06:05
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief	2019-01-30 02:25
Articles in Press	2019-01-30 02:25
Publication Fee Transferred
Edit the Manuscript by Language Editor	2019-02-03 02:53
Typeset the Manuscript	2019-02-26 02:22
Publish the Manuscript Online	2019-02-26 09:05

ISSN	2307-8960 (online)
Open Access	This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is 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/
Copyright	© The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved.
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Category	Medicine, Research & Experimental
Manuscript Type	Case Report
Article Title	Recurrent acute liver failure associated with novel SCYL1 mutation: A case report
Manuscript Source	Unsolicited Manuscript
All Author List	Jia-Qi Li, Jing-Yu Gong, A S Knisely, Mei-Hong Zhang and Jian-She Wang
ORCID	Author(s) ORCID Number Jia-Qi Li http://orcid.org/0000-0002-3150-3212 Jing-Yu Gong http://orcid.org/0000-0002-1149-0979 A S Knisely http://orcid.org/0000-0002-9173-539X Mei-Hong Zhang http://orcid.org/0000-0001-9656-7180 Jian-She Wang http://orcid.org/0000-0003-0823-586X
Funding Agency and Grant Number	Funding Agency Grant Number National Natural Science Foundation of China 81570468
Corresponding Author	Jian-She Wang, MD, PhD, Professor, The Center for Pediatric Liver Diseases, Children’s Hospital of Fudan University, 399 Wanyuan Road, Minhang District, Shanghai 201102, China. jshwang@shmu.edu.cn
Key Words	SCYL1; Recurrent acute liver failure; Whole-exome sequencing; Case report
Core Tip	An infant or child with recurrent acute liver failure may have biallelic mutation in SCYL1. A search for causes should include evaluation of this gene even if neurologic or skeletal disease is not appreciated.
Publish Date	2019-02-26 09:05
Citation	Li JQ, Gong JY, Knisely AS, Zhang MH, Wang JS. Recurrent acute liver failure associated with novel SCYL1 mutation: A case report. World J Clin Cases 2019; 7(4): 494-499
URL	https://www.wjgnet.com/2307-8960/full/v7/i4/494.htm
DOI	https://dx.doi.org/10.12998/wjcc.v7.i4.494

Full Article (PDF)	WJCC-7-494.pdf
Full Article (Word)	WJCC-7-494.docx
CARE Checklist–2016	43213-CARE-Checklist–2016-revision.pdf
Manuscript File	43213-Review_Edited.docx
Answering Reviewers	43213-Answering reviewers.pdf
Audio Core Tip	43213-Audio core tip.wma
Conflict-of-Interest Disclosure Form	43213-Conflict-of-interest statement.pdf
Copyright License Agreement	43213-Copyright license agreement.pdf
Approved Grant Application Form(s) or Funding Agency Copy of any Approval Document(s)	43213-Grant application form(s).pdf
Signed Informed Consent Form(s) or Document(s)	43213-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	43213-Language certificate.pdf
Supplementary Material	43213-Supplementary material.pdf
Peer-review Report	43213-Peer-review(s).pdf
Scientific Misconduct Check	43213-Scientific misconduct check.pdf
Scientific Editor Work List	43213-Scientific editor work list.pdf
CrossCheck Report	43213-CrossCheck report.pdf