Publication Name	World Journal of Clinical Cases
Manuscript ID	71782
Country	China

Received	2021-09-22 12:16
Peer-Review Started	2021-09-22 12:18
To Make the First Decision
Return for Revision	2022-01-10 09:03
Revised	2022-01-23 12:04
Second Decision	2022-03-29 02:02
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief	2022-04-04 05:05
Articles in Press	2022-04-04 05:05
Publication Fee Transferred
Edit the Manuscript by Language Editor	2022-03-23 01:38
Typeset the Manuscript	2022-04-27 02:27
Publish the Manuscript Online	2022-05-24 14:32

ISSN	2307-8960 (online)
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Category	Hematology
Manuscript Type	Case Report
Article Title	Targeted next-generation sequencing identifies a novel nonsense mutation in ANK1 for hereditary spherocytosis: A case report
Manuscript Source	Unsolicited Manuscript
All Author List	Pan Fu, Yang-Yang Jiao, Kai Chen, Jing-Bo Shao, Xue-Lian Liao, Jing-Wei Yang and Sha-Yi Jiang
ORCID	Author(s) ORCID Number Jing-Bo Shao http://orcid.org/0000-0002-1451-8033 Sha-Yi Jiang http://orcid.org/0000-0002-6734-9122
Funding Agency and Grant Number	Funding Agency Grant Number the Natural Science Foundation of Shanghai Science Committee 18ZR1431200 Research Foundation of Shanghai Municipal Health Commission 20194Y0112 Clinical Research Plan of SHDC SHDC2020CR4089
Corresponding Author	Sha-Yi Jiang, MD, PhD, Chief Physician, Department of Hematology and Oncology, Shanghai Children’s Hospital, Shanghai Jiao Tong University, No. 355 Luding Road, Shanghai 200062, China. jiangshayi@163.com
Key Words	Hereditary spherocytosis; ANK1 mutation; Next-generation sequencing; Case report; Nonsense mutation
Core Tip	We report a case of hereditary spherocytosis. The clinical manifestation and a mutation of ANK1 gene (exon23: c.G2467T:p.E823X) were assessed and related literature was reviewed. The information in this report may help with the diagnosis of hereditary spherocytosis.
Publish Date	2022-05-24 14:32
Citation	Fu P, Jiao YY, Chen K, Shao JB, Liao XL, Yang JW, Jiang SY. Targeted next-generation sequencing identifies a novel nonsense mutation in ANK1 for hereditary spherocytosis: A case report. World J Clin Cases 2022; 10(15): 4923-4928
URL	https://www.wjgnet.com/2307-8960/full/v10/i15/4923.htm
DOI	https://dx.doi.org/10.12998/wjcc.v10.i15.4923

Full Article (PDF)	WJCC-10-4923.pdf
Full Article (Word)	WJCC-10-4923.docx
Manuscript File	71782_Auto_Edited-YJM-Filipodia.docx
Answering Reviewers	71782-Answering reviewers.pdf
Audio Core Tip	71782-Audio core tip.m4a
Conflict-of-Interest Disclosure Form	71782-Conflict-of-interest statement.pdf
Copyright License Agreement	71782-Copyright license agreement.pdf
Signed Consent for Treatment Form(s) or Document(s)	71782-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	71782-Language certificate.pdf
Peer-review Report	71782-Peer-review(s).pdf
Scientific Editor Work List	71782-Scientific editor work list.pdf
CrossCheck Report	71782-CrossCheck report.pdf