Predominantly myalgic phenotype caused by the c.3466G>A p.A1156T mutation in SCN4A gene

Johanna Palmio, Satu Sandell, Michael Hanna, Roope Männikkö, Sini Penttilä, Bjarne Udd

    Research output: Contribution to journalArticleScientificpeer-review

    15 Citations (Scopus)
    Original languageEnglish
    Pages (from-to)1520-1527
    JournalNeurology
    Volume88
    Issue number16
    DOIs
    Publication statusPublished - 2017
    Publication typeA1 Journal article-refereed

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