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384 related items for PubMed ID: 23498838

  • 1. S4153R is a gain-of-function mutation in the cardiac Ca(2+) release channel ryanodine receptor associated with catecholaminergic polymorphic ventricular tachycardia and paroxysmal atrial fibrillation.
    Zhabyeyev P, Hiess F, Wang R, Liu Y, Wayne Chen SR, Oudit GY.
    Can J Cardiol; 2013 Aug; 29(8):993-6. PubMed ID: 23498838
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  • 7. Mutant ryanodine receptors in catecholaminergic polymorphic ventricular tachycardia generate delayed afterdepolarizations due to increased propensity to Ca2+ waves.
    Paavola J, Viitasalo M, Laitinen-Forsblom PJ, Pasternack M, Swan H, Tikkanen I, Toivonen L, Kontula K, Laine M.
    Eur Heart J; 2007 May; 28(9):1135-42. PubMed ID: 17347175
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  • 16. Complex atrial arrhythmias as first manifestation of catecholaminergic polymorphic ventricular tachycardia: an unusual course in a patient with a new mutation in ryanodine receptor type 2 gene.
    Lawrenz W, Krogmann ON, Wieczorek M.
    Cardiol Young; 2014 Aug; 24(4):741-4. PubMed ID: 23985380
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  • 17. Ryanodine receptors and ventricular arrhythmias: emerging trends in mutations, mechanisms and therapies.
    George CH, Jundi H, Thomas NL, Fry DL, Lai FA.
    J Mol Cell Cardiol; 2007 Jan; 42(1):34-50. PubMed ID: 17081562
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  • 18. Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia.
    Marks AR, Priori S, Memmi M, Kontula K, Laitinen PJ.
    J Cell Physiol; 2002 Jan; 190(1):1-6. PubMed ID: 11807805
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