NaV1.4 Channel[2]
[1]. Markgraf R, et al. Mechanism and molecular basis for the sodium channel subtype specificity of μ-conopeptide CnIIIC. Br J Pharmacol. 2012 Oct;167(3):576-86.
[2]. Del Río-Sancho S, et al. Cutaneous iontophoresis of μ-conotoxin CnIIIC-A potent NaV1.4 antagonist with analgesic, anaesthetic and myorelaxant properties. Int J Pharm. 2017 Feb 25;518(1-2):59-65.
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