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Muscle Channelopathies: the Nondystrophic Myotonias and Periodic Paralyses
PURPOSE OF REVIEW: The muscle channelopathies are a group of rare inherited diseases caused by mutations in muscle ion channels. Mutations cause an increase or decrease in muscle membrane excitability, leading to a spectrum of related clinical disorders: the nondystrophic myotonias are characterized...
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| 出版年: | Continuum (Minneap Minn) |
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| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
American Academy of Neurology
2013
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4234136/ https://ncbi.nlm.nih.gov/pubmed/24305449 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/01.CON.0000440661.49298.c8 |
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