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Articles Published Processes
7/11/2022 8:36:00 AM | Browse: 364 | Download: 1317
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Received |
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2021-06-25 02:26 |
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Peer-Review Started |
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2021-06-25 02:26 |
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First Decision by Editorial Office Director |
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2021-09-01 10:35 |
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Return for Revision |
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2021-09-01 10:35 |
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Revised |
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2021-09-16 14:48 |
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Publication Fee Transferred |
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Second Decision by Editor |
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2022-06-10 03:05 |
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Second Decision by Editor-in-Chief |
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Final Decision by Editorial Office Director |
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2022-06-17 22:24 |
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Articles in Press |
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2022-06-17 22:24 |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2022-07-03 08:55 |
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Publish the Manuscript Online |
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2022-07-11 08:36 |
| 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/ |
| 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 |
Genetics & Heredity |
| Manuscript Type |
Case Report |
| Article Title |
Updated clinical and glycomic features of mannosyl-oligosaccharide glucosidase deficiency: Two case reports
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| Manuscript Source |
Unsolicited Manuscript |
| All Author List |
Kuerbanjiang Abuduxikuer, Lei Wang, Lin Zou, Cui-Yan Cao, Long Yu, Hong-Mei Guo, Xin-Miao Liang, Jian-She Wang and Li Chen |
| ORCID |
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| Funding Agency and Grant Number |
| Funding Agency |
Grant Number |
| National Science and Technology Major Project |
2014ZX09101046-004 |
| National Natural Science Foundation of China |
81873543 |
| National Natural Science Foundation of China |
81570468 |
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| Corresponding Author |
Jian-She Wang, MD, PhD, Professor, Department of Hepatology, Children's Hospital of Fudan University, No. 399 Wanyuan Road, Shanghai 201102, China. jshwang@shmu.edu.cn |
| Key Words |
Mannosyl-oligosaccharide glucosidase; MOGS-CDG; Congenital disorder of glycosylation type IIb; Mannosyl-oligosaccharide glucosidase gene; Glycomics of IgG1; Case report |
| Core Tip |
We updated the clinical and glycosylation features of 2 previously published patients with mannosyl-oligosaccharide glucosidase-congenital disorders of glycosylation (MOGS-CDG) by confirming abnormal glycomics and expanding the phenotypical and glycomic spectrum of MOGS-CDG. We also postulated a compensatory glycosylation pathway, leading to a possible serum biomarker for future diagnosis. |
| Publish Date |
2022-07-11 08:36 |
| Citation |
Abuduxikuer K, Wang L, Zou L, Cao CY, Yu L, Guo HM, Liang XM, Wang JS, Chen L. Updated clinical and glycomic features of mannosyl-oligosaccharide glucosidase deficiency: Two case reports. World J Clin Cases 2022; 10(21): 7397-7408
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| URL |
https://www.wjgnet.com/2307-8960/full/v10/i21/7397.htm |
| DOI |
https://dx.doi.org/10.12998/wjcc.v10.i21.7397 |
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