A Korean family with Arg1448Cys mutation of SCN4A channel causing paramyotonia congenita: electrophysiologic, histopathologic, and molecular genetic studies.

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Published in J Korean Med Sci on December 01, 2002

Authors

Dae-Seong Kim1, Eun-Joo Kim, Dae-Soo Jung, Kyu-Hyun Park, In-Joo Kim, Ki-Young Kwak, Cheol-Min Kim, Hyun-Yoon Ko

Author Affiliations

1: Department of Neurology, College of Medicine, Pusan National University, Busan, Korea. kimcm@hyowon.cc.pusan.ac.kr

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