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1 Electrophysiological characteristics of R47W and A298T mutations in CLC-1 of myotonia congenita patients and evaluation of clinical features
Hyung Jin Chin, Chan Hyeong Kim, Kotdaji Ha, Jin Hong Shin, Dae-Seong Kim, Insuk So
Korean J Physiol Pharmacol.2017;21(4):439-447.   Published online 2017 June 26     DOI: http://dx.doi.org/10.4196/kjpp.2017.21.4.439
      
2 The Overlap between Fibromyalgia Syndrome and Myotonia Congenita
Tai-Seung Nam, Seok-Yong Choi, Dong-Jin Park, Shin-Seok Lee, Young-Ok Kim, Myeong-Kyu Kim
J Clin Neurol.2015;11(2):188-191.   Published online 2014 November 11     DOI: http://dx.doi.org/10.3988/jcn.2015.11.2.188
      
3 Clinical Characteristics and Analysis of CLCN1 in Patients with "EMG Disease"
Tai-Seung Nam, Hyun-Jung Jung, Seok-Yong Choi, Young-Ok Kim, Myeong-Kyu Kim, Ki-Hyun Cho
J Clin Neurol.2012;8(3):212-217.   Published online 2012 September 27     DOI: http://dx.doi.org/10.3988/jcn.2012.8.3.212
      
4 Novel CLCN1 Mutations and Clinical Features of Korean Patients with Myotonia Congenita
In-Soo Moon, Hyang-Sook Kim, Jin-Hong Shin, Yeong-Eun Park, Kyu-Hyun Park, Yong-Bum Shin, Jong Seok Bae, Young-Chul Choi, Dae-Seong Kim
J Korean Med Sci.2009;24(6):1038-1044.   Published online 2009 November 9     DOI: http://dx.doi.org/10.3346/jkms.2009.24.6.1038
      

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