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Journal Abstract Search

567 related items for PubMed ID: 9425895

  • 1. A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.
    Singh NA, Charlier C, Stauffer D, DuPont BR, Leach RJ, Melis R, Ronen GM, Bjerre I, Quattlebaum T, Murphy JV, McHarg ML, Gagnon D, Rosales TO, Peiffer A, Anderson VE, Leppert M.
    Nat Genet; 1998 Jan; 18(1):25-9. PubMed ID: 9425895
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  • 2. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.
    Charlier C, Singh NA, Ryan SG, Lewis TB, Reus BE, Leach RJ, Leppert M.
    Nat Genet; 1998 Jan; 18(1):53-5. PubMed ID: 9425900
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  • 7. A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family.
    Lee WL, Biervert C, Hallmann K, Tay A, Dean JC, Steinlein OK.
    Neuropediatrics; 2000 Feb; 31(1):9-12. PubMed ID: 10774989
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  • 10. A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions.
    Ishii A, Fukuma G, Uehara A, Miyajima T, Makita Y, Hamachi A, Yasukochi M, Inoue T, Yasumoto S, Okada M, Kaneko S, Mitsudome A, Hirose S.
    Brain Dev; 2009 Jan; 31(1):27-33. PubMed ID: 18640800
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  • 11. Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy.
    Schroeder BC, Kubisch C, Stein V, Jentsch TJ.
    Nature; 1998 Dec 17; 396(6712):687-90. PubMed ID: 9872318
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  • 13. A novel splicing mutation in KCNQ2 in a multigenerational family with BFNC followed for 25 years.
    de Haan GJ, Pinto D, Carton D, Bader A, Witte J, Peters E, van Erp G, Vandereyken W, Boezeman E, Wapenaar MC, Boon P, Halley D, Koeleman BP, Lindhout D.
    Epilepsia; 2006 May 17; 47(5):851-9. PubMed ID: 16686649
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  • 15. KCNQ2, the first gene found to be mutated in human generalized idiopathic epilepsy.
    Steinlein OK, Jentsch TJ.
    Pathol Biol (Paris); 1998 Nov 17; 46(9):683-4. PubMed ID: 9885816
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  • 16. KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes.
    Neubauer BA, Waldegger S, Heinzinger J, Hahn A, Kurlemann G, Fiedler B, Eberhard F, Muhle H, Stephani U, Garkisch S, Eeg-Olofsson O, Müller U, Sander T.
    Neurology; 2008 Jul 15; 71(3):177-83. PubMed ID: 18625963
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  • 17. [Benign familial neonatal convulsions: a model of idiopathic epilepsy].
    Hirsch E, de Saint-Martin A, Marescaux C.
    Rev Neurol (Paris); 1999 Jul 15; 155(6-7):463-7. PubMed ID: 10472660
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