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    • Functional Analysis of a Novel Potassium Channel (KCNA1) Mutation in Hereditary Mokymia 

      Chen, Haijun; von Hehn, Christian A.; Kaczmarek, Leonard K.; Ment, Laura R.; Pober, Barbara R.; Hisama, Fuki Marie (Springer-Verlag, 2007)
      Myokymia is characterized by spontaneous, involuntary muscle fiber group contraction visible as vermiform movement of the overlying skin. Myokymia with episodic ataxia is a rare, autosomal dominant trait caused by mutations ...