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Articles Published Processes
2/26/2019 9:05:12 AM | Browse: 1117 | Download: 2146
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Received |
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2018-11-20 02:31 |
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Peer-Review Started |
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2018-11-20 08:24 |
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First Decision by Editorial Office Director |
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2018-12-20 05:06 |
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Return for Revision |
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2019-01-03 01:15 |
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Revised |
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2019-01-16 12:34 |
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Publication Fee Transferred |
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Second Decision by Editor |
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2019-01-29 06:05 |
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Second Decision by Editor-in-Chief |
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Final Decision by Editorial Office Director |
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2019-01-30 02:25 |
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Articles in Press |
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2019-01-30 02:25 |
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Edit the Manuscript by Language Editor |
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2019-02-03 02:53 |
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Typeset the Manuscript |
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2019-02-26 02:22 |
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Publish the Manuscript Online |
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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. |
| Article Reprints |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
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| Permissions |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
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| Publisher |
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA |
| Website |
http://www.wjgnet.com |
| Category |
Medicine, Research & Experimental |
| Manuscript Type |
Case Report |
| Article Title |
Recurrent acute liver failure associated with novel SCYL1 mutation: A case report
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| Manuscript Source |
Unsolicited Manuscript |
| All Author List |
Jia-Qi Li, Jing-Yu Gong, A S Knisely, Mei-Hong Zhang and Jian-She Wang |
| ORCID |
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| Funding Agency and Grant Number |
| Funding Agency |
Grant Number |
| National Natural Science Foundation of China |
81570468 |
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| 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 |
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