| 1 | SCN4A, HOKPP2
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| Mutation screening in Chinese hypokalemic periodic paralysis patients.
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| Wang W, Jiang L, Ye L, Zhu N, Su T, Guan L, Li X, Ning G.
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| Mol Genet Metab 87(4):359-63. Epub 2006 Jan 4. 2006
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| 2 | HOKPP2
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| Correlating phenotype and genotype in the periodic paralyses.
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| 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.
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| Neurology 63(9):1647-55. 2004
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| 3 | HOKPP2, SCN4A
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| Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current.
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| 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.
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| Proc Natl Acad Sci U S A 97(17):9549-54. 2000
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| 4 | HOKPP2, SCN4A
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| A novel sodium channel mutation causing hypokalemic periodic paralysis. (abstr)
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| Bulman DE, et al.
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| Am J Hum Genet 61 : A327. 1997
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