SCN4A基因R672G位点突变致低钾性周期性瘫痪伴肌萎缩一家系分析并文献复习
夏钰, 沙倩倩, 朱雯华, 乔凯, 都爱莲
The clinical and pathological characteristics of a hypokalemic periodic paralysis family with muscle atrophy due to SCN4A R672G mutation and review of literatures
XIA Yu, SHA Qian-qian, ZHU Wen-hua, QIAO Kai, DU Ai-lian
中国现代神经疾病杂志
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2022, (8): 717
-722
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DOI: 10.3969/j.issn.1672-6731.2022.08.011
