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6. Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutations. Plassart E, Reboul J, Rime CS, Recan D, Millasseau P, Eymard B, Pelletier J, Thomas C, Chapon F, Desnuelle C. Eur J Hum Genet; 1994 Aug; 2(2):110-24. PubMed ID: 8044656 [Abstract] [Full Text] [Related]
7. Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysis. Ptacek LJ, Gouw L, Kwieciński H, McManis P, Mendell JR, Barohn RJ, George AL, Barchi RL, Robertson M, Leppert MF. Ann Neurol; 1993 Mar; 33(3):300-7. PubMed ID: 8388676 [Abstract] [Full Text] [Related]
15. Periodic paralysis, myotonia congenita and sarcolemmal ion channels: a success of the candidate gene approach. Fontaine B. Neuromuscul Disord; 1993 Mar; 3(2):101-7. PubMed ID: 7689379 [Abstract] [Full Text] [Related]