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Articles Published Processes
1/14/2025 8:49:30 AM | Browse: 43 | Download: 146
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Received |
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2024-08-24 16:53 |
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Peer-Review Started |
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2024-08-24 16:53 |
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To Make the First Decision |
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Return for Revision |
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2024-11-18 08:19 |
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Revised |
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2024-11-30 15:13 |
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Second Decision |
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2024-12-20 03:07 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2024-12-20 07:32 |
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Articles in Press |
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2024-12-20 07:32 |
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Publication Fee Transferred |
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Edit the Manuscript by Language Editor |
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2024-12-24 11:32 |
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Typeset the Manuscript |
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2024-12-30 04:35 |
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Publish the Manuscript Online |
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2025-01-14 08:49 |
ISSN |
2220-3206 (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) 2024. 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 |
Clinical Neurology |
Manuscript Type |
Retrospective Cohort Study |
Article Title |
Sodium channel mutation SCN1A T875M, D188V and associated dysfunction with drug resistant epilepsy
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Manuscript Source |
Invited Manuscript |
All Author List |
Pradeep Kumar Dabla, Swapan Gupta, Swati Singh, Aroop Viswas, Manisha Yadav, Subash Chandra Sonkar and Bidhan Chandra Koner |
ORCID |
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Funding Agency and Grant Number |
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Corresponding Author |
Pradeep Kumar Dabla, MBBS, MD, Professor, Department of Biochemistry, Govind Ballabh Pant Institute of Postgraduate Medical Education and Research, 1, Jawaharlal Nehru Marg, 64 Khamba, Raj Ghat, New Delhi 110002, Delhi, India. pradeep_dabla@yahoo.com |
Key Words |
Epilepsy; Single nucleotide polymorphisms; Drug-resistant epilepsy; SCN1A receptor; SCN1A rs121918623 and SCN1A rs121917953 gene polymorphism |
Core Tip |
Epilepsy is the most common paroxysmal neurological disorder with significant global health burden. A subset of patients are resistant to anti-epileptic drugs, leading to increased mortality and decreased quality of life. Mutations in genes encoding neuronal voltage-gated sodium channels have been linked to inherited forms of epilepsy. This study investigates the correlation between SCN1A gene variants rs121918623 and SCN1A rs121917953 and drug resistance in epilepsy suggesting specific genotypes as potential biomarkers in drug-resistant idiopathic epilepsy. |
Publish Date |
2025-01-14 08:49 |
Citation |
<p>Dabla PK, Gupta S, Singh S, Viswas A, Yadav M, Sonkar SC, Koner BC. Sodium channel mutation SCN1A T875M, D188V and associated dysfunction with drug resistant epilepsy. <i>World J Psychiatry</i> 2025; 15(2): 100738</p> |
URL |
https://www.wjgnet.com/2220-3206/full/v15/i2/100738.htm |
DOI |
https://dx.doi.org/10.5498/wjp.v15.i2.100738 |
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