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

doi:10.3969/j.issn.1672-6731.2022.08.011

Home>Articles>The clinical and pathological characteristics of a hypokalemic periodic paralysis family with muscle atrophy due to SCN4A R672G mutation and review of literatures

DOI: 10.3969/j.issn.1672-6731.2022.08.011

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

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Publication Date：2022-08-25

Online Publishing Date：2025-08-15(First online date of this platform, not the publication date of the document)

Pages：6( 717-722 )

Chinese Journal of Contemporary Neurology and Neurosurgery

ISTICPKU

ISSN：1672-6731

Year, Vol.(Issue)：2022,22(8)