Clinical and genetic features of SCN4A-T704M mutation-related normokalemic periodic paralysis：A report of two Chinese families and mechanism of phenotypic heterogeneity

XIONG Qianqian, DING Weijiang, LI Xueming

Journal of Apoplexy and Nervous Diseases ›› 2026, Vol. 43 ›› Issue (1) : 70-75.

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Journal of Apoplexy and Nervous Diseases ›› 2026, Vol. 43 ›› Issue (1) : 70-75. DOI: 10.19845/j.cnki.zfysjjbzz.2026.0012
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Clinical and genetic features of SCN4A-T704M mutation-related normokalemic periodic paralysis：A report of two Chinese families and mechanism of phenotypic heterogeneity

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{{article.zuoZheEn_L}}. {{article.title_en}}[J]. {{journal.qiKanMingCheng_EN}}, 2026, 43(1): 70-75 https://doi.org/10.19845/j.cnki.zfysjjbzz.2026.0012

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