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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...
Guardat en:
| Publicat a: | J Physiol |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2017
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| Matèries: | |
| Accés en línia: | 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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