SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes Fertleman et al. (2006) Neuron 52: 767–774
No takes yet. Share an insight, caveat, or question.
F. I. YOUNG (2007) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: