메뉴 건너뛰기




Volumn 24, Issue 5, 2013, Pages 570-572

The contradictory genetics of atrial fibrillation: The growing gap between knowledge and clinical implications

Author keywords

atrial fibrillation; familial; genetics; R231H; single nucleotide polymorphisms

Indexed keywords

MITOCHONDRIAL DNA; POTASSIUM CHANNEL KCNE1; POTASSIUM CHANNEL KCNQ1;

EID: 84876887617     PISSN: 10453873     EISSN: 15408167     Source Type: Journal    
DOI: 10.1111/jce.12091     Document Type: Note
Times cited : (3)

References (18)
  • 3
    • 0000297776 scopus 로고
    • Familial auricular fibrillation
    • Wolf L,: Familial auricular fibrillation. N Engl J Med 1943; 229396-229398.
    • (1943) N Engl J Med , pp. 229396-229398
    • Wolf, L.1
  • 5
    • 80052726709 scopus 로고    scopus 로고
    • The genetics of atrial fibrillation: From the bench to the bedside
    • Xiao J, Liang D, Chen YH,: The genetics of atrial fibrillation: From the bench to the bedside. Annu Rev Genomics Hum Genet 2011; 12:73-96.
    • (2011) Annu Rev Genomics Hum Genet , pp. 1273-1296
    • Xiao, J.1    Liang, D.2    Chen, Y.H.3
  • 6
    • 84871242129 scopus 로고    scopus 로고
    • New advances in the genetic basis of atrial fibrillation
    • Mahida S, Ellinor PT,; New advances in the genetic basis of atrial fibrillation. J Cardiovasc Electrophysiol 2012; 23: 1400-1406.
    • (2012) J Cardiovasc Electrophysiol , vol.23 , pp. 1400-1406
    • Mahida, S.1    Ellinor, P.T.2
  • 7
    • 0037331522 scopus 로고    scopus 로고
    • Atrial fibrillation is associated with accumulation of aging-related common type mitochondrial DNA deletion mutation in human atrial tissue
    • Lai LP, Tsai CC, Su MJ, Lin JL, Chen YS, Tseng YZ, Huang SK,: Atrial fibrillation is associated with accumulation of aging-related common type mitochondrial DNA deletion mutation in human atrial tissue. Chest 2003; 123: 539-544.
    • (2003) Chest , vol.123 , pp. 539-544
    • Lai, L.P.1    Tsai, C.C.2    Su, M.J.3    Lin, J.L.4    Chen, Y.S.5    Tseng, Y.Z.6    Huang, S.K.7
  • 10
    • 10344258576 scopus 로고    scopus 로고
    • Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation
    • Ellinor PT, Moore RK, Patton KK, Ruskin JN, Pollak MR, Macrae CA,: Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation. Heart 2004; 90: 1487-1488.
    • (2004) Heart , vol.90 , pp. 1487-1488
    • Ellinor, P.T.1    Moore, R.K.2    Patton, K.K.3    Ruskin, J.N.4    Pollak, M.R.5    MacRae, C.A.6
  • 14
    • 84863996184 scopus 로고    scopus 로고
    • ATX-II-induced pulmonary vein arrhythmogenesis related to atrial fibrillation and long QT syndrome
    • Lu YY, Cheng CC, Chen YC, Chen SA, Chen YJ,: ATX-II-induced pulmonary vein arrhythmogenesis related to atrial fibrillation and long QT syndrome. Eur J Clin Invest 2012; 42: 823-831.
    • (2012) Eur J Clin Invest , vol.42 , pp. 823-831
    • Lu, Y.Y.1    Cheng, C.C.2    Chen, Y.C.3    Chen, S.A.4    Chen, Y.J.5
  • 18
    • 73249124602 scopus 로고    scopus 로고
    • Monitoring of atrial fibrillation burden after surgical ablation: Relevancy of end-point criteria after radiofrequency ablation treatment of patients with lone atrial fibrillation
    • Beukema R, Beukema WP, Sie HT, Misier AR, Delnoy PP, Elvan A,: Monitoring of atrial fibrillation burden after surgical ablation: Relevancy of end-point criteria after radiofrequency ablation treatment of patients with lone atrial fibrillation. Interact Cardiovasc Thorac Surg 2009; 9: 956-959.
    • (2009) Interact Cardiovasc Thorac Surg , vol.9 , pp. 956-959
    • Beukema, R.1    Beukema, W.P.2    Sie, H.T.3    Misier, A.R.4    Delnoy, P.P.5    Elvan, A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.