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Query Trace: Hypokalemic Periodic Paralysis and SCN4A[orginal query]

Novel susceptibility gene for nonfamilial hypokalemic periodic paralysis. Neurology 2016 Mar . Song I-Wen, Sung Chih-Chien, Chen Chien-Hsiun, Cheng Chih-Jen, Yang Sung-Sen, Chou Yi-Chun, Yang Jenn-Hwai, Chen Yuan-Tsong, Wu Jer-Yuarn, Lin Shih-H Similar articles in PubMed
Mutations of SCN4A gene cause different diseases: 2 case reports and literature review. Channels (Austin, Tex.) 2015 9 (2): 82-7. Liu Xiao-li, Huang Xiao-jun, Luan Xing-hua, Zhou Hai-yan, Wang Tian, Wang Jing-yi, Chen Sheng-di, Tang Hui-dong, Cao Similar articles in PubMed
Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype. Neurology 2011 Nov 77 (22): 1960-4. Matthews E, Portaro S, Ke Q, Sud R, Haworth A, Davis M B, Griggs R C, Hanna M Similar articles in PubMed
Absence of ion channels CACN1AS and SCN4A mutations in thyrotoxic hypokalemic periodic paralysis. Thyroid : official journal of the American Thyroid Association 2004 Mar 14 (3): 187-90. Ng WY, Lui KF, Thai AC, Cheah JS Similar articles in PubMed