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A Novel SCN9A Mutation Responsible for Primary Erythromelalgia and Is Resistant to the Treatment of Sodium Channel Blockers

Primary erythromelalgia (PE) is an autosomal dominant neurological disorder characterized by severe burning pain and erythema in the extremities upon heat stimuli or exercise. Mutations in human SCN9A gene, encoding the α–subunit of the voltage-gated sodium channel, Na(v)1.7, were found to be respon...

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Bibliografiska uppgifter
Huvudupphovsmän: Wu, Min-Tzu, Huang, Po-Yuan, Yen, Chen-Tung, Chen, Chih-Cheng, Lee, Ming-Jen
Materialtyp: Artigo
Språk:Inglês
Publicerad: Public Library of Science 2013
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Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3561374/
https://ncbi.nlm.nih.gov/pubmed/23383113
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0055212
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