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APA Citation
Habbout, K., Poulin, H., Rivier, F., Giuliano, S., Sternberg, D., Fontaine, B., Eymard, B., Morales, R. J., Echenne, B., King, L., Hanna, M. G., Männikkö, R., Chahine, M., Nicole, S., & Bendahhou, S. (2016). a recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis. Neurology, 86, . http://access.bl.uk/ark:/81055/vdc_100041977527.0x00005b