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

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
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.
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

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 Company 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

ISSN	2307-8960 (online)
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