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Elevated resting H(+) current in the R1239H type 1 hypokalaemic periodic paralysis mutated Ca(2+) channel
KEY POINTS: Missense mutations in the gene encoding the α1 subunit of the skeletal muscle voltage‐gated Ca(2+) channel induce type 1 hypokalaemic periodic paralysis, a poorly understood neuromuscular disease characterized by episodic attacks of paralysis associated with low serum K(+). Acute express...
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| 發表在: | J Physiol |
|---|---|
| Main Authors: | , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
John Wiley and Sons Inc.
2017
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5638893/ https://ncbi.nlm.nih.gov/pubmed/28857175 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/JP274638 |
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