Predominantly myalgic phenotype caused by the c.3466G>A p.A1156T mutation in <i>SCN4A</i> gene
Johanna Palmio, Bjarne Udd(Folkhälsans Forskningscentrum), Michael G. Hanna(National Hospital for Neurology and Neurosurgery), Roope Männikkö(National Hospital for Neurology and Neurosurgery), Satu Sandell(Seinäjoki University of Applied Sciences), Sini Penttilä(Tampere University)
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