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Volumn 144, Issue 1, 2010, Pages 149-151

Role of the R1135H KCNH2 mutation in Brugada syndrome

Author keywords

Action potentials; Brugada syndrome; Computer simulation; Delayed rectifier potassium channels; KCNH2; Short QT syndrome

Indexed keywords

POTASSIUM CHANNEL; POTASSIUM CHANNEL KCNH2; UNCLASSIFIED DRUG;

EID: 77957862142     PISSN: 01675273     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijcard.2008.12.177     Document Type: Article
Times cited : (29)

References (7)
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    • H. Itoh, T. Sakaguchi, and T. Ashihara A novel KCNH2 mutation as a modifier for short QT interval Int J Cardiol 137 2009 83 85
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  • 2
    • 33846627787 scopus 로고    scopus 로고
    • Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death
    • C. Antzelevitch, G.D. Pollevick, and J.M. Cordeiro Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death Circulation 115 2007 442 449
    • (2007) Circulation , vol.115 , pp. 442-449
    • Antzelevitch, C.1    Pollevick, G.D.2    Cordeiro, J.M.3
  • 3
    • 33645317063 scopus 로고    scopus 로고
    • HERG potassium channels and cardiac arrhythmia
    • M.C. Sanguinetti, and M. Tristani-Firouzi hERG potassium channels and cardiac arrhythmia Nature 440 2006 463 469
    • (2006) Nature , vol.440 , pp. 463-469
    • Sanguinetti, M.C.1    Tristani-Firouzi, M.2
  • 4
    • 27644573433 scopus 로고    scopus 로고
    • Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome
    • A.O. Verkerk, R. Wilders, and E. Schulze-Bahr Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome Cardiovasc Res 68 2005 441 453
    • (2005) Cardiovasc Res , vol.68 , pp. 441-453
    • Verkerk, A.O.1    Wilders, R.2    Schulze-Bahr, E.3
  • 5
    • 0034473172 scopus 로고    scopus 로고
    • Cellular and ionic mechanisms responsible for the Brugada syndrome
    • C. Antzelevitch, and G.X. Yan Cellular and ionic mechanisms responsible for the Brugada syndrome J Electrocardiol 33 suppl 1 2000 33 39
    • (2000) J Electrocardiol , vol.33 , Issue.SUPPL. 1 , pp. 33-39
    • Antzelevitch, C.1    Yan, G.X.2
  • 6
    • 0037044399 scopus 로고    scopus 로고
    • Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males
    • J.M. Di Diego, J.M. Cordeiro, and R.J. Goodrow Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males Circulation 106 2002 2004 2011
    • (2002) Circulation , vol.106 , pp. 2004-2011
    • Di Diego, J.M.1    Cordeiro, J.M.2    Goodrow, R.J.3
  • 7
    • 57549110416 scopus 로고    scopus 로고
    • Ethical authorship and publishing
    • A.J. Coats Ethical authorship and publishing Int J Cardiol 131 2009 149 150
    • (2009) Int J Cardiol , vol.131 , pp. 149-150
    • Coats, A.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.