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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Vydáno v:J Physiol
Hlavní autoři: Fuster, Clarisse, Perrot, Jimmy, Berthier, Christine, Jacquemond, Vincent, Allard, Bruno
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2017
Témata:
Molecular and Cellular
On-line přístup: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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