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收藏分享 收藏 Notched T waves on Holter recordings enhance detection of patients with LQT2 (HERG) mutations
Lupoglazoff, JM; Denjoy, I; Berthet, M; Neyroud, N; Demay, L; Richard, P; Hainque, B; Vaksmann, G; Klug, D; Leenhardt, A; Maillard, G; Coumel, P; Guicheney, P 分享 收藏 分享 收藏 C-terminal HERG mutations -: The role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrenceBerthet, M; Denjoy, I; Donger, C; Demay, L; Hammoude, H; Klug, D; Schulze-Bahr, E; Richard, P; Funke, H; Schwartz, K; Coumel, P; Hainque, B; Guicheney, P 分享 收藏 Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndromeNeyroud, N; Richard, P; Vignier, N; Donger, C; Denjoy, I; Demay, L; Shkolnikova, M; Pesce, R; Chevalier, P; Hainque, B; Coumel, P; Schwartz, K; Guicheney, P 分享 收藏 分享 收藏 分享 收藏 Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndromeNeyroud, N; Denjoy, I; Donger, C; Gary, F; Villain, E; Leenhardt, A; Benali, K; Schwartz, K; Coumel, P; Guicheney, P 分享 收藏 KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndromeDonger, C; Denjoy, I; Berthet, M; Neyroud, N; Cruaud, C; Bennaceur, M; Chivoret, G; Schwartz, K; Coumel, P; Guicheney, P 分享 收藏 A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndromeNeyroud, N; Tesson, F; Denjoy, I; Leibovici, M; Donger, C; Barhanin, J; Faure, S; Gary, F; Coumel, P; Petit, C; Schwartz, K; Guicheney, P 分享 收藏 分享 收藏 分享 收藏 
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