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Authors
Chen, Limin
Zhang, Hongbo
Li, Chunnv
Yang, Nuo
Wang, Jiangtao
Liang, Jianmin https://orcid.org/0000-0003-0117-0207
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Funding
Funding for this research was provided by:
the National Nature and Science Foundation of China (No.82271509, No.81771396)
the Foundation of Jilin Provincial Key Laboratory of Pediatric Neurology (No. YDZJ202102CXJD021)
the Project of Jilin Provincial Science and Technology Development Plan (No.YDZJ202201ZYTS676)
Natural Science Foundation of Jilin Province (No. YDZJ202201ZYTS090)
the Project of Jilin Medical and Health Talents (No.JLSWSRCZX2021053)
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Article History
Received: 24 October 2024
Revised: 23 November 2024
Accepted: 26 November 2024
First Online: 12 December 2024
Declarations
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: The authors declare that they have no conflict of interest.
: This study was approved by the Ethics Committee of Bethune First Hospital of Jilin University. Informed consent was obtained from all the participants and their legal guardian involved in the study.
: Written informed consent from all the participants and patient’s parents was obtained before conducting the gene test, including the patient’s clinical and EMG details in the manuscript for publication.
