Publication Name	World Journal of Clinical Cases
Manuscript ID	67278
Country	China

Received	2021-04-20 03:29
Peer-Review Started	2021-04-20 03:32
To Make the First Decision
Return for Revision	2021-07-15 11:01
Revised	2021-08-09 04:35
Second Decision	2021-09-18 03:29
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2021-09-19 08:42
Articles in Press	2021-09-19 08:42
Publication Fee Transferred
Edit the Manuscript by Language Editor	2021-10-09 12:58
Typeset the Manuscript	2021-11-15 06:12
Publish the Manuscript Online	2021-11-22 10:34

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	Pediatrics
Manuscript Type	Case Report
Article Title	Novel KDM6A mutation in a Chinese infant with Kabuki syndrome: A case report
Manuscript Source	Unsolicited Manuscript
All Author List	Hong-Xian Guo, Bao-Wei Li, Mei Hu, Shao-Yan Si and Kai Feng
ORCID	Author(s) ORCID Number Hong-Xian Guo http://orcid.org/0000-0001-5301-0374 Bao-Wei Li http://orcid.org/0000-0003-4907-6674 Mei Hu http://orcid.org/0000-0001-7767-1089 Shao-Yan Si http://orcid.org/0000-0002-3948-7712 Kai Feng http://orcid.org/0000-0003-1493-1650
Funding Agency and Grant Number
Corresponding Author	Kai Feng, MD, Director, Special Medical Center, Strategic Support Force Medical Center of PLA, No. 9 North Anxiang Road, Chaoyang District, Beijing 100101, China. fkjiafp@126.com
Key Words	Kabuki syndrome; KDM6A; Gene mutation; Chinese; Case report
Core Tip	The case report describes a de novo KDM6A mutation in a Chinese patient with Kabuki syndrome (KS). This novel KDM6A frame-shift mutation further broadened the KS mutation spectrum and knowledge of its clinical manifestations.
Publish Date	2021-11-22 10:34
Citation	Guo HX, Li BW, Hu M, Si SY, Feng K. Novel KDM6A mutation in a Chinese infant with Kabuki syndrome: A case report. World J Clin Cases 2021; 9(33): 10257-10264
URL	https://www.wjgnet.com/2307-8960/full/v9/i33/10257.htm
DOI	https://dx.doi.org/10.12998/wjcc.v9.i33.10257

Full Article (PDF)	WJCC-9-10257.pdf
Full Article (Word)	WJCC-9-10257.docx
CARE Checklist–2016	67278-CARE-Checklist–2016-revision.pdf
Manuscript File	67278_Auto_Edited-SYB_Kerr C_Clear Copy.docx
Answering Reviewers	67278-Answering reviewers.pdf
Audio Core Tip	67278-Audio core tip.m4a
Conflict-of-Interest Disclosure Form	67278-Conflict-of-interest statement.pdf
Copyright License Agreement	67278-Copyright license agreement.pdf
Signed Informed Consent Form(s) or Document(s)	67278-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	67278-Language certificate.pdf
Peer-review Report	67278-Peer-review(s).pdf
Scientific Editor Work List	67278-Scientific editor work list.pdf