Mutations in sodium-channel gene SCN9A cause a spectrum of human genetic pain disorders
J. Clin. Invest. Joost P.H. Drenth , et al. 117:3603 doi:10.1172/JCI33297 [
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Figure 2Neuronal Na
v1.7 channels.
Na
v1.7 (shown here in red after immunocytostaining with anti-Nav1.7 antibody; Alomone Reagents) within the tip of a growing neurite from rat DRG neuron in culture. Image kindly provided by Joel A. Black, Department of Neurology, Yale University, New Haven, Connecticut, USA.