| 1 | KCNJ18, THYPOKKP2 |
| 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. | |
| J Biol Chem 286(31):27425-35. Epub 2011 Jun 10. Erratum in: J Biol Chem. 2011 Sep 23;286(38):33707. 2011 | |
| 2 | KCNJ18, THYPOKPP2 |
| Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis. | |
| Ryan DP, da Silva MR, Soong TW, Fontaine B, Donaldson MR, Kung AW, Jongjaroenprasert W, Liang MC, Khoo DH, Cheah JS, Ho SC, Bernstein HS, Maciel RM, Brown RH Jr, Ptácek LJ. | |
| Cell 140(1):88-98. 2010 | |