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1 A Korean Family with Arg1448Cys Mutation of SCN4A Channel Causing Paramyotonia Congenita: Electrophysiologic, Histopathologic, and Molecular Genetic Studies
Dae Seong Kim, Eun Joo Kim, Dae Soo Jung, Kyu Hyun Park, In Joo Kim, Ki Young Kwak, Cheol Min Kim, Hyun Yoon Ko
J Korean Med Sci.2002;17(6):856-860.   Published online 2009 April 23     DOI: http://dx.doi.org/10.3346/jkms.2002.17.6.856
      
2 Gene-to-Gene Interaction between Sodium Channel-Related Genes in Determining the Risk of Antiepileptic Drug Resistance
Sin-Young Jang, Myeong-Kyu Kim, Kee-Ra Lee, Man-Seok Park, Byeong-Chae Kim, Ki-Hyun Cho, Min-Cheol Lee, Yo-Sik Kim
J Korean Med Sci.2009;24(1):62-68.   Published online 2009 February 28     DOI: http://dx.doi.org/10.3346/jkms.2009.24.1.62
      
3 The Genotype and Clinical Phenotype of Korean Patients with Familial Hypokalemic Periodic Paralysis
June-Bum Kim, Man-Ho Kim, Soon Ju Lee, Dae-Joong Kim, Byung Churl Lee
J Korean Med Sci.2007;22(6):946-951.   Published online 2007 December 20     DOI: http://dx.doi.org/10.3346/jkms.2007.22.6.946
      
4 A Family with A Missense Mutation in the SCN5A Gene
Chang Ho Shin, Nam Ho Kim, Kyung Hee Kim, Su Sung Yoo, Yong Bock Choi, Seok Kyu Oh, Kyeong Man Hong, Jin Won Jeong, Moon Kee Paik
Korean Circ J.2003;33(2):150-154.   Published online 2003 February 28     DOI: http://dx.doi.org/10.4070/kcj.2003.33.2.150
      

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