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PUBMED FOR HANDHELDS

Journal Abstract Search


198 related items for PubMed ID: 1654742

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  • 2. Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17.
    Koch MC, Ricker K, Otto M, Grimm T, Bender K, Zoll B, Harper PS, Lehmann-Horn F, Rüdel R, Hoffman EP.
    Hum Genet; 1991 Nov; 88(1):71-4. PubMed ID: 1660029
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  • 4. Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locus.
    Ptacek LJ, Tyler F, Trimmer JS, Agnew WS, Leppert M.
    Am J Hum Genet; 1991 Aug; 49(2):378-82. PubMed ID: 1651050
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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
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  • 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
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  • 9. Linkage of hyperkalaemic periodic paralysis in quarter horses to the horse adult skeletal muscle sodium channel gene.
    Rudolph JA, Spier SJ, Byrns G, Hoffman EP.
    Anim Genet; 1992 Mar; 23(3):241-50. PubMed ID: 1323940
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  • 12. Linkage of atypical myotonia congenita to a sodium channel locus.
    Ptacek LJ, Tawil R, Griggs RC, Storvick D, Leppert M.
    Neurology; 1992 Feb; 42(2):431-3. PubMed ID: 1310531
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  • 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
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  • 18. Identification of a mutation in the gene causing hyperkalemic periodic paralysis.
    Ptácek LJ, George AL, Griggs RC, Tawil R, Kallen RG, Barchi RL, Robertson M, Leppert MF.
    Cell; 1991 Nov 29; 67(5):1021-7. PubMed ID: 1659948
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