Publication Name	World Journal of Clinical Cases
Manuscript ID	70743
Country	China

Received	2021-08-14 02:50
Peer-Review Started	2021-08-14 02:53
First Decision by Editorial Office Director	2021-09-29 07:20
Return for Revision	2021-09-29 07:20
Revised	2021-10-10 03:15
Publication Fee Transferred
Second Decision by Editor	2021-11-16 03:29
Second Decision by Editor-in-Chief
Final Decision by Editorial Office Director	2021-11-18 06:38
Articles in Press	2021-11-18 06:38
Edit the Manuscript by Language Editor	2021-11-07 22:57
Typeset the Manuscript	2021-12-09 03:23
Publish the Manuscript Online	2021-12-23 14:14

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	De novo mutation loci and clinical analysis in a child with sodium taurocholate cotransport polypeptide deficiency: A case report
Manuscript Source	Unsolicited Manuscript
All Author List	Hui-Yan Liu, Meng Li and Qi Li
ORCID	Author(s) ORCID Number Hui-Yan Liu http://orcid.org/0000-0002-6940-1633 Meng Li http://orcid.org/0000-0002-2908-635X Qi Li http://orcid.org/0000-0002-9012-4562
Funding Agency and Grant Number	Funding Agency Grant Number Yunnan Science Foundation Project No. 2019-81960102.
Corresponding Author	Qi Li, PhD, Professor, Department of Pediatrics, the First Affiliated Hospital of Kunming Medical University , No. 295 Xichang Road, Kunming 650000, Yunnan Province, China. 412289442@qq.com
Key Words	Sodium taurocholate cotransport polypeptide; SLC10A1 gene; Hypercholesterolemia; Behavioral neurodevelopmental delay; Children; Case report
Core Tip	The mutation loci and clinical manifestations of sodium taurocholate cotransport polypeptide deficiency disease are currently under further investigation. Our case emphasizes the need to re-examine the clinical manifestations, prognosis and interventions associated with hypercholesterolemia due to this disease and suggests that behavioral neurodevelopmental delay may also be a clinical manifestation of this disease.
Publish Date	2021-12-23 14:14
Citation	Liu HY, Li M, Li Q. De novo mutation loci and clinical analysis in a child with sodium taurocholate cotransport polypeptide deficiency: A case report. World J Clin Cases 2021; 9(36): 11487-11494
URL	https://www.wjgnet.com/2307-8960/full/v9/i36/11487.htm
DOI	https://dx.doi.org/10.12998/wjcc.v9.i36.11487

Full Article (PDF)	WJCC-9-11487.pdf
Full Article (Word)	WJCC-9-11487.docx
Manuscript File	70743_Auto_Edited.docx
Answering Reviewers	70743-Answering reviewers.pdf
Audio Core Tip	70743-Audio core tip.mp4
Conflict-of-Interest Disclosure Form	70743-Conflict-of-interest statement.pdf
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Non-Native Speakers of English Editing Certificate	70743-Language certificate.pdf
Peer-review Report	70743-Peer-review(s).pdf
Scientific Misconduct Check	70743-CrossCheck.png
Scientific Editor Work List	70743-Scientific editor work list.pdf
CrossCheck Report	70743-CrossCheck report.pdf