Functional analysis of missense variants in the TRESK (KCNK18) K(+) channel

A loss of function mutation in the TRESK K2P potassium channel (KCNK18), has recently been linked with typical familial migraine with aura. We now report the functional characterisation of additional TRESK channel missense variants identified in unrelated patients. Several variants either had no app...

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Bibliografiset tiedot
Päätekijät: Andres-Enguix, Isabelle, Shang, Lijun, Stansfeld, Phillip J., Morahan, Julia M., Sansom, Mark S. P., Lafrenière, Ronald G., Roy, Bishakha, Griffiths, Lyn R., Rouleau, Guy A., Ebers, George C., Cader, Zameel M., Tucker, Stephen J.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Nature Publishing Group 2012
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3266952/
https://ncbi.nlm.nih.gov/pubmed/22355750
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep00237
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