Palmio, J., Sandell, S., Hanna, M. G., Männikkö, R., Penttilä, S., & Udd, B. (2017). Predominantly myalgic phenotype caused by the c.3466G>A p.A1156T mutation in SCN4A gene. Neurology.

Palmio, Johanna, Satu Sandell, Michael G. Hanna, Roope Männikkö, Sini Penttilä, and Bjarne Udd. "Predominantly Myalgic Phenotype Caused By the C.3466G>A P.A1156T Mutation in SCN4A Gene." Neurology 2017.

Palmio, Johanna, et al. "Predominantly Myalgic Phenotype Caused By the C.3466G>A P.A1156T Mutation in SCN4A Gene." Neurology 2017.