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

por Kim, Dae-Seong, Kim, Eun-Joo, Jung, Dae-Soo, Park, Kyu-Hyun, Kim, In-Joo, Kwak, Ki-Young, Kim, Cheol-Min, Ko, Hyun-Yoon
Publicado 2002