Citations for
1SCN4A, HOKPP2
Mutation screening in Chinese hypokalemic periodic paralysis patients.
Wang W, Jiang L, Ye L, Zhu N, Su T, Guan L, Li X, Ning G.
Mol Genet Metab 87(4):359-63. Epub 2006 Jan 4. 2006
2HOKPP2
Correlating phenotype and genotype in the periodic paralyses.
Miller TM, Dias da Silva MR, Miller HA, Kwiecinski H, Mendell JR, Tawil R, McManis P, Griggs RC, Angelini C, Servidei S, Petajan J, Dalakas MC, Ranum LP, Fu YH, Ptacek LJ.
Neurology 63(9):1647-55. 2004
3HOKPP2, SCN4A
Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current.
Jurkat-Rott K, Mitrovic N, Hang C, Kouzmekine A, Iaizzo P, Herzog J, Lerche H, Nicole S, Vale-Santos J, Chauveau D, Fontaine B, Lehmann-Horn F.
Proc Natl Acad Sci U S A 97(17):9549-54. 2000
4HOKPP2, SCN4A
A novel sodium channel mutation causing hypokalemic periodic paralysis. (abstr)
Bulman DE, et al.
Am J Hum Genet 61 : A327. 1997