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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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Vydáno v:Continuum (Minneap Minn)
Hlavní autoři: Statland, Jeffrey M., Barohn, Richard J.
Médium: Artigo
Jazyk:Inglês
Vydáno: American Academy of Neurology 2013
Témata:
On-line přístup: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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