Cor Vasa 2012, 54(3-4):e84-e87 | DOI: 10.1016/j.crvasa.2012.03.003
Mutation analysis of RyR2 gene in patients after arrhythmic storm
- a Interní kardiologická klinika, Fakultní nemocnice Brno, Brno, Česká republika
- b Oddělení lékařské genetiky, Fakultní nemocnice Brno, Brno, Česká republika
Keywords: Arrhythmic storm; Mutation analysis; RyR2 gene; Sudden cardiac death
Received: February 11, 2012; Revised: March 7, 2012; Accepted: March 7, 2012; Published: March 1, 2012 Show citation
References
- Myerburg RJ, Wellens HJJ. Epidemiology of Cardiac Arrest. In: Priori SG, Zipes DP (Eds.). Sudden Cardiac Death: A handbook for clinical practice. Oxford: Blackwell Publishing Ltd., 2006:3-17.
Go to original source...
- Moss AJ, Zareba W, Hall WJ, et al; for the Multicenter Automatic Defibrillator Implantation Trial II investigators. Prophylactic implantation of a defibrillator in patients with myocardial infarction and reduced ejection fraction. N Engl J Med 2002;346:877-83.
Go to original source...
Go to PubMed...
- Friedlander Y, Siscovick DS, Weinmann S, Austin MA, Psaty BM, Lemaitre RN, et al. Family history as a risk factor for primary cardiac arrest. Circulation 1998;97:155-60.
Go to original source...
Go to PubMed...
- Jouvan X, Desnos M, Guerot C, Ducimetière P. Predicting sudden death in the population: The Paris Prospective Study I. Circulation 1999;99:1978-83.
Go to original source...
Go to PubMed...
- Kaikkonen KS, Kortelainen ML, Linna E, Huikuri HV. Family history and the risk of sudden cardiac death as a manifestation of an acute coronary event. Circulation 2006;114:1462-7.
Go to original source...
Go to PubMed...
- Dekker LR, Bezzina CR, Henriques JP, Tanck MW, Koch KT, Alings MW, et al. Familial sudden death is an important risk factor for primary ventricular fibrillation: A casecontrol study in acute myocardial infarction patients. Circulation 2006;114:1140-5.
Go to original source...
Go to PubMed...
- Priori SG, Chen W. Inherited dysfunction of sarcoplasmic reticulum Ca2+ handling and arrhythmogenesis. Circ Res 2011;108:871-83.
Go to original source...
Go to PubMed...
- Bagattin A, Veronese C, Bauce B, Wuyts W, Settimo L, Nava A, et al. Denaturing HPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmias. Clinical Chemistry 2004;50:1148-55.
Go to original source...
Go to PubMed...
- Medeiros-DA, Bhuiyan ZA, Tester DJ, Hofman N, Bikker H, vanTintelen P, et al. The RYR2-encoded ryanodine receptor/calcium channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome. J Am Coll Cardiol 2009;54:2065-74.
Go to original source...
Go to PubMed...
- Postma AV, Denjoy I, Kamblock J, Alders M, Lupoglazoff JM, Vaksmann G, et al. Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and folow up of the patients. J Med Genet 2005;42:863-70.
Go to original source...
Go to PubMed...
- Bagattin A, Veronese C, Rampazzo A, Danieli GA. Gene symbol: RYR2. Disease: Effort-induced polymorphic ventricular arrhythmias. Hum Genet 2004;114):404-5.
Go to PubMed...
- Ensembl release 65 - Dec 2011. http://www.ensembl.org/Homo_sapiens/Info/Index
- Stecker EC, Sono M, Wallace E, Gunson K, Jui J, Chugh SS. Allelic variants of SCN5A and risk of sudden cardiac arrest in patients with coronary artery disease. Heart Rhythm 2006;3:697-700.
Go to original source...
Go to PubMed...
- Albert CM, Nam EG, Rimm EB, Jin HW, Hajjar RJ, Hunter DJ, et al. Cardiac sodium channel gene variants and sudden cardiac death in women. Circulation 2008;117:16-23.
Go to original source...
Go to PubMed...
- Novotný T, Kadlecová J, Raudenská M, Bittnerová A, Andršová I, Floriánová A, et al. Mutation Analysis Ion Channel Genes Ventricular Fibrillation Survivors with Coronary Artery Disease. PACE 2011,34:742-9.
Go to original source...
Go to PubMed...
- George GH, Jundi H, Thomas NL, Scoote M, Walters N, Williams AJ, et al. Ryanodine receptor regulation by intramolecular interaction between cytoplasmic and transmembrane domains. Mol Biol Cell 2004;15:2627-38.
Go to original source...
Go to PubMed...