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Open Access

Expanding the Allelic spectrum in ATP1A3-related disorders with 3 novel mutations and clinic features

Suad A. Alyamani, Hesham M. Aldhalaan, Mohammed A. Almuhaizea and Musaad F. Abukhalid
Neurosciences Journal July 2023, 28 (3) 195-198; DOI: https://doi.org/10.17712/nsj.2023.3.20220131
Suad A. Alyamani
From the Department of Neuroscience Centre, King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia
MD
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  • For correspondence: [email protected]
Hesham M. Aldhalaan
From the Department of Neuroscience Centre, King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia
MD
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Mohammed A. Almuhaizea
From the Department of Neuroscience Centre, King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia
MD
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Musaad F. Abukhalid
From the Department of Neuroscience Centre, King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia
MD
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Article Information

vol. 28 no. 3 195-198
DOI 
https://doi.org/10.17712/nsj.2023.3.20220131
PubMed 
37482377

Published By 
Neurosciences Journal
Online ISSN 
1658-3183
History 
  • Received December 21, 2022
  • Accepted June 13, 2023
  • Published online July 23, 2023.

Copyright & Usage 
Copyright: © Neurosciences Neurosciences is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work.

Author Information

  1. Suad A. Alyamani, MD⇑,
  2. Hesham M. Aldhalaan, MD,
  3. Mohammed A. Almuhaizea, MD and
  4. Musaad F. Abukhalid, MD
  1. From the Department of Neuroscience Centre, King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia
  1. Address correspondence and reprint request to: Dr. Suad Alyamani, Department of Neuroscience Centre, King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia. E-mail: suadalya{at}gmail.com
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  • Childhood-related neural genotype–phenotype in ATP1A3 mutations: comprehensive analysis
    Osama Y. Muthaffar, Asma Alqarni, Jumana A. Shafei, Sarah Y. Bahowarth, Anas S. Alyazidi, Muhammad Imran Naseer
    Genes & Genomics 2024 46 4
  • Subjective cognitive decline in conjunction with cerebrospinal fluid anti-ATP1A3 autoantibodies and a low amyloid β 1–42/1–40 ratio: Report and literature review
    Niels Hansen, Kristin Rentzsch, Anne Elisa Sagebiel, Sina Hirschel, Björn Hendrik Schott, Dirk Fitzner, Jens Wiltfang, Claudia Bartels
    Behavioural Brain Research 2025 485
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Neurosciences Journal: 28 (3)
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Vol. 28, Issue 3
1 Jul 2023
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Expanding the Allelic spectrum in ATP1A3-related disorders with 3 novel mutations and clinic features
Suad A. Alyamani, Hesham M. Aldhalaan, Mohammed A. Almuhaizea, Musaad F. Abukhalid
Neurosciences Journal Jul 2023, 28 (3) 195-198; DOI: 10.17712/nsj.2023.3.20220131

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Expanding the Allelic spectrum in ATP1A3-related disorders with 3 novel mutations and clinic features
Suad A. Alyamani, Hesham M. Aldhalaan, Mohammed A. Almuhaizea, Musaad F. Abukhalid
Neurosciences Journal Jul 2023, 28 (3) 195-198; DOI: 10.17712/nsj.2023.3.20220131
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© 2025 Neurosciences Journal Neurosciences is copyright under the Berne Convention and the International Copyright Convention. All rights reserved. Neurosciences is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work. Electronic ISSN 1658-3183. Print ISSN 1319-6138.

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