Publication Name	World Journal of Clinical Cases
Manuscript ID	69482
Country	China

Received	2021-07-01 12:18
Peer-Review Started	2021-07-01 12:21
To Make the First Decision
Return for Revision	2021-07-16 02:38
Revised	2021-07-21 13:29
Second Decision	2021-09-09 03:19
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2021-09-10 09:16
Articles in Press	2021-09-10 09:16
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2021-10-29 01:37
Publish the Manuscript Online	2021-11-10 01:44

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	Rare mutation in MKRN3 in two twin sisters with central precocious puberty: Two case reports
Manuscript Source	Unsolicited Manuscript
All Author List	Li-Qiong Jiang, Yan-Qiong Zhou, Ke Yuan, Jian-Fang Zhu, Yan-Lan Fang and Chun-Lin Wang
ORCID	Author(s) ORCID Number Li-Qiong Jiang http://orcid.org/0000-0001-5918-1430 Yan-Qiong Zhou http://orcid.org/0000-0003-2281-0234 Ke Yuan http://orcid.org/0000-0002-0458-3683 Jian-Fang Zhu http://orcid.org/0000-0002-1580-0479 Yan-Lan Fang http://orcid.org/0000-0001-6579-417X Chun-Lin Wang http://orcid.org/0000-0002-8288-3075
Funding Agency and Grant Number	Funding Agency Grant Number the key Research and Development Program of Zhejiang Province 2020C03121
Corresponding Author	Chun-Lin Wang, MD, PhD, Chief Doctor, Department of Pediatrics, The First Affiliated Hospital, Zhejiang University School of Medicine, No. 79 Qingchun Road, Hangzhou 310003, Zhejiang Province, China. hzwangcl@zju.edu.cn
Key Words	Central precocious puberty; MKRN3; Mutation; Case report
Core Tip	This report discusses the diagnosis and treatment of central precocious puberty caused by a new Makorin ring finger protein 3 gene mutation and includes a detailed clinical and laboratory analysis of the pathogenic principle, which provided the diagnosis and led to the treatment of central precocious puberty.
Publish Date	2021-11-10 01:44
Citation	Jiang LQ, Zhou YQ, Yuan K, Zhu JF, Fang YL, Wang CL. Rare mutation in MKRN3 in two twin sisters with central precocious puberty: Two case reports. World J Clin Cases 2021; 9(32): 10018-10023
URL	https://www.wjgnet.com/2307-8960/full/v9/i32/10018.htm
DOI	https://dx.doi.org/10.12998/wjcc.v9.i32.10018

Full Article (PDF)	WJCC-9-10018.pdf
Full Article (Word)	WJCC-9-10018.docx
CARE Checklist–2016	69482-CARE-Checklist–2016-revision.pdf
Manuscript File	69482_Auto_Edited.docx
Answering Reviewers	69482-Answering reviewers.pdf
Audio Core Tip	69482-Audio core tip.m4a
Conflict-of-Interest Disclosure Form	69482-Conflict-of-interest statement.pdf
Copyright License Agreement	69482-Copyright license agreement.pdf
Approved Grant Application Form(s) or Funding Agency Copy of any Approval Document(s)	69482-Grant application form(s).pdf
Signed Informed Consent Form(s) or Document(s)	69482-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	69482-Language certificate.pdf
Peer-review Report	69482-Peer-review(s).pdf
Scientific Misconduct Check	69482-Bing-Wang JJ-2.png
Scientific Editor Work List	69482-Scientific editor work list.pdf