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Volumn 25, Issue 5, 2014, Pages 522-530

Gain-of-function KCNH2 mutations in patients with Brugada syndrome

Author keywords

Brugada syndrome; KCNH2; mutation; patch clamp; ventricular tachycardia

Indexed keywords

POTASSIUM CHANNEL; POTASSIUM CHANNEL KCNH2; SODIUM CHANNEL NAV1.5; UNCLASSIFIED DRUG; CACNA1C PROTEIN, HUMAN; CALCIUM CHANNEL L TYPE; ERG1 POTASSIUM CHANNEL; POTASSIUM CHANNEL HERG; SCN5A PROTEIN, HUMAN;

EID: 84899644025     PISSN: 10453873     EISSN: 15408167     Source Type: Journal    
DOI: 10.1111/jce.12361     Document Type: Article
Times cited : (36)

References (23)
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    • Priori SG, Wilde AA, Horie M, Cho Y, Behr ER, Berul C, Blom N, Brugada J, Chiang CE, Huikuri H, Kannankeril P, Krahn A, Leenhardt A, Moss A, Schwartz PJ, Shimizu W, Tomaselli G, Tracy C,: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: Expert consensus statement on inherited primary arrhythmia syndromes: Document endorsed by HRS, EHRA, and APHRS in may 2013 and by ACCF, AHA, PACES, and AEPC in June 2013. Heart Rhythm 2013: e75-e106.
    • (2013) Heart Rhythm
    • Priori, S.G.1    Wilde, A.A.2    Horie, M.3    Cho, Y.4    Behr, E.R.5    Berul, C.6    Blom, N.7    Brugada, J.8    Chiang, C.E.9    Huikuri, H.10    Kannankeril, P.11    Krahn, A.12    Leenhardt, A.13    Moss, A.14    Schwartz, P.J.15    Shimizu, W.16    Tomaselli, G.17    Tracy, C.18
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    • Biophysical characterization of the short QT mutation hERG-N588K reveals a mixed gain-and loss-of-function
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  • 17
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    • Role of the R1135H KCNH2 mutation in Brugada syndrome
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.