Na leak with gating pore properties in hypokalemic periodic paralysis V876E mutant muscle Ca channel

Type 1 hypokalemic periodic paralysis (HypoPP1) is a poorly understood genetic neuromuscular disease characterized by episodic attacks of paralysis associated with low blood K(+). The vast majority of HypoPP1 mutations involve the replacement of an arginine by a neutral residue in one of the S4 segm...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:J Gen Physiol
Päätekijät: Fuster, Clarisse, Perrot, Jimmy, Berthier, Christine, Jacquemond, Vincent, Charnet, Pierre, Allard, Bruno
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: The Rockefeller University Press 2017
Aiheet:
Research Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5715907/
https://ncbi.nlm.nih.gov/pubmed/29114033
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1085/jgp.201711834
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