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Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis
BACKGROUND: Several missense mutations of CACNA1S and SCN4A genes occur in hypokalemic periodic paralysis. These mutations affect arginine residues in the S4 voltage sensors of the channel. Approximately 20% of cases remain genetically undefined. METHODS: We undertook direct automated DNA sequencing...
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| Main Authors: | , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Academy of Neurology
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2848101/ https://ncbi.nlm.nih.gov/pubmed/19118277 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/01.wnl.0000342387.65477.46 |
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