Overlap of periodic paralysis and paramyotonia congenita caused by SCN4A gene mutations two family reports and literature review
Author:
Affiliation:
1. First Clinical Medical College, Shanxi Medical University, Taiyuan, China
2. Department of Neurology, First Affiliated Hospital, Shanxi Medical University, Taiyuan, China
Funder
No funding
Publisher
Informa UK Limited
Subject
Biochemistry,Biophysics
Link
https://www.tandfonline.com/doi/pdf/10.1080/19336950.2019.1600967
Reference28 articles.
1. The exercise test in periodic paralysis
2. Electromyography guides toward subgroups of mutations in muscle channelopathies
3. Exercise test in muscle channelopathies and other muscle disorders
4. Channelopathies of Skeletal Muscle Excitability
5. Ding ZY. The value of exercise test in the diagnosis of primary periodic paralysis [Doctoral dissertation]. Peking Union Medical College; 2008. Chinese.
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