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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...

詳細記述

保存先:
書誌詳細
主要な著者: Wu, Min-Tzu, Huang, Po-Yuan, Yen, Chen-Tung, Chen, Chih-Cheng, Lee, Ming-Jen
フォーマット: Artigo
言語:Inglês
出版事項: Public Library of Science 2013
主題:
オンライン・アクセス: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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