Cite
HARVARD Citation
Habbout, K. et al. (2016). A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis. Neurology. p. . [Online].
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Habbout, K. et al. (2016). A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis. Neurology. p. . [Online].