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Skeletal Muscle Channelopathies: New insights into the periodic paralyses and nondystrophic myotonias
PURPOSE OF REVIEW: To summarize advances in our understanding of the clinical phenotypes, genetics, and molecular pathophysiology of the periodic paralyses, the nondystrophic myotonias, and other muscle channelopathies. RECENT FINDINGS: The number of pathogenic mutations causing periodic paralysis,...
Tallennettuna:
| Päätekijät: | , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2009
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2763141/ https://ncbi.nlm.nih.gov/pubmed/19571750 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/WCO.0b013e32832efa8f |
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