Article info
Neurogenetics
Original research
Clinical and genetic analysis of familial neuromyelitis optica spectrum disorder in Chinese: associated with ubiquitin-specific peptidase USP18 gene variants
- Correspondence to Professor Wei Qiu, Department of Neurology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China; qiuwei{at}mail.sysu.edu.cn; Dr. Qingfen Yu, Department of Neurology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China; yuqf5{at}mail.sysu.edu.cn
Citation
Clinical and genetic analysis of familial neuromyelitis optica spectrum disorder in Chinese: associated with ubiquitin-specific peptidase USP18 gene variants
Publication history
- Received May 19, 2022
- Accepted August 15, 2022
- First published September 1, 2022.
Online issue publication
May 24, 2023
Article Versions
- Previous version (14 November 2022).
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© Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.