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2009•Neuromuscular DisordersRequires access

G.P.14.08 Analysis of the CLCN1 gene in Czech patients with myotonia congenita

Jana Sedláčková, Stanislav Voháňka, Markéta Hermanová, Petr Vondráček, Lenka Fajkusová

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Key concepts: Myotonia congenita, Channelopathy, Myotonia, Genetics, Gene, Mutation, Biology, Internal medicine

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