2 results  1 of 1 

1 Familial Hemiplegic Migraine with Prolonged Coma and Cerebellar Atrophy: CACNA1A T666M Mutation in a Korean Family
Kyung-Ho Choi, Jang Su Kim, Seo-Young Lee, Suk-won Ryu, Sam Su Kim, Seung-hwan Lee, Sunghun Kim, Hee-Kwon Park
J Korean Med Sci.2012;27(9):1124-1127.   Published online 2012 August 22     DOI: http://dx.doi.org/10.3346/jkms.2012.27.9.1124
      
2 Episodic Ataxia Type 2 due to a Deletion Mutation in the CACNA1A Gene in a Korean Family
Jeong-Min Kim, Ji Soo Kim, Chang-Seok Ki, Beom-Seok Jeon
J Clin Neurol.2006;2(4):268-271.   Published online 2006 December 20     DOI: http://dx.doi.org/10.3988/jcn.2006.2.4.268
      

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