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Articles Published Processes
5/24/2022 2:32:32 PM | Browse: 443 | Download: 1217
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Received |
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2021-09-22 12:16 |
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Peer-Review Started |
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2021-09-22 12:18 |
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First Decision by Editorial Office Director |
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2022-01-10 09:03 |
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Return for Revision |
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2022-01-10 09:03 |
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Revised |
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2022-01-23 12:04 |
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Publication Fee Transferred |
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Second Decision by Editor |
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2022-03-29 02:02 |
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Second Decision by Editor-in-Chief |
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Final Decision by Editorial Office Director |
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2022-04-04 05:05 |
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Articles in Press |
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2022-04-04 05:05 |
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Edit the Manuscript by Language Editor |
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2022-03-23 01:38 |
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Typeset the Manuscript |
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2022-04-27 02:27 |
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Publish the Manuscript Online |
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2022-05-24 14:32 |
| 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: https://creativecommons.org/Licenses/by-nc/4.0/ |
| Copyright |
©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. |
| Article Reprints |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
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| Permissions |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
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| Publisher |
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA |
| Website |
http://www.wjgnet.com |
| 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
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| 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 |
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| 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 |
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| 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 |
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