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Recent Advances in the Pathogenesis and Drug Action in Periodic Paralyses and Related Channelopathies
The periodic paralysis (PP) are rare autosomal-dominant disorders associated to mutations in the skeletal muscle sodium, calcium, and potassium channel genes characterized by muscle fiber depolarization with un-excitability, episodes of weakness with variations in serum potassium concentrations. Rec...
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| Autori principali: | , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Frontiers Research Foundation
2011
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3108473/ https://ncbi.nlm.nih.gov/pubmed/21687503 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphar.2011.00008 |
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