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A calcium channel mutant mouse model of hypokalemic periodic paralysis
Hypokalemic periodic paralysis (HypoPP) is a familial skeletal muscle disorder that presents with recurrent episodes of severe weakness lasting hours to days associated with reduced serum potassium (K(+)). HypoPP is genetically heterogeneous, with missense mutations of a calcium channel (Ca(V)1.1) o...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Clinical Investigation
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3533564/ https://ncbi.nlm.nih.gov/pubmed/23187123 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI66091 |
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