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Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis.
Cell. 2010 Jan 8;140(1):88-98. doi: 10.1016/j.cell.2009.12.024.
Cell. 2010.
PMID: 20074522
Free PMC article.
Identification and functional characterization of Kir2.6 mutations associated with non-familial hypokalemic periodic paralysis.
Cheng CJ, Lin SH, Lo YF, Yang SS, Hsu YJ, Cannon SC, Huang CL.
Cheng CJ, et al.
J Biol Chem. 2011 Aug 5;286(31):27425-35. doi: 10.1074/jbc.M111.249656. Epub 2011 Jun 10.
J Biol Chem. 2011.
PMID: 21665951
Free PMC article.
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