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Journal Abstract Search

214 related items for PubMed ID: 1659948

  • 1. 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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  • 7. Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the adult muscle sodium channel gene.
    Ebers GC, George AL, Barchi RL, Ting-Passador SS, Kallen RG, Lathrop GM, Beckmann JS, Hahn AF, Brown WF, Campbell RD.
    Ann Neurol; 1991 Dec 29; 30(6):810-6. PubMed ID: 1686388
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  • 8. 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 29; 33(3):300-7. PubMed ID: 8388676
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  • 11. Identification of a Thr-to-Met mutation in the skeletal muscle sodium channel gene in hyperkalemic periodic paralysis of a Japanese family.
    Arahata K, Wang J, Feero WG, Hayakawa H, Honda K, Sugita H, Hoffman EP.
    Ann N Y Acad Sci; 1993 Dec 20; 707():342-5. PubMed ID: 9137564
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  • 12. A Met-to-Val mutation in the skeletal muscle Na+ channel alpha-subunit in hyperkalaemic periodic paralysis.
    Rojas CV, Wang JZ, Schwartz LS, Hoffman EP, Powell BR, Brown RH.
    Nature; 1991 Dec 05; 354(6352):387-9. PubMed ID: 1659668
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  • 13. Hyperkalemic periodic paralysis caused by recurring mutation in the adult muscle sodium channel alpha-subunit gene.
    Sillén A, Wadelius C, Sundvall M, Ahlsten G, Gustavson KH.
    Genet Couns; 1996 Dec 05; 7(4):267-75. PubMed ID: 8985730
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  • 14. 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 05; 49(2):378-82. PubMed ID: 1651050
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  • 15. Hyperkalemic periodic paralysis with cardiac dysrhythmia: a novel sodium channel mutation?
    Baquero JL, Ayala RA, Wang J, Curless RG, Feero WG, Hoffman EP, Ebeid MR.
    Ann Neurol; 1995 Mar 05; 37(3):408-11. PubMed ID: 7695243
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  • 16. 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 05; 88(1):71-4. PubMed ID: 1660029
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  • 20. Dinucleotide repeat polymorphisms at the SCN4A locus suggest allelic heterogeneity of hyperkalemic periodic paralysis and paramyotonia congenita.
    McClatchey AI, Trofatter J, McKenna-Yasek D, Raskind W, Bird T, Pericak-Vance M, Gilchrist J, Arahata K, Radosavljevic D, Worthen HG.
    Am J Hum Genet; 1992 May 05; 50(5):896-901. PubMed ID: 1315122
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