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Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation
Augustus O. Grant, Michael P. Carboni, Valentina Neplioueva, C. Frank Starmer, Mirella Memmi, Carlo Napolitano, Silvia Priori
Augustus O. Grant, Michael P. Carboni, Valentina Neplioueva, C. Frank Starmer, Mirella Memmi, Carlo Napolitano, Silvia Priori
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Article

Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation

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Abstract

Research Article

Authors

Augustus O. Grant, Michael P. Carboni, Valentina Neplioueva, C. Frank Starmer, Mirella Memmi, Carlo Napolitano, Silvia Priori

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Figure 7

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Comparison of the late component of Na+ current in the wild-type and ΔK1...
Comparison of the late component of Na+ current in the wild-type and ΔK1500 mutant Na+ channels. (a and b) The Na+ current was recorded at high gain (upper trace) and low gain (lower trace) with 200-ms pulses from a holding potential of –100 mV to a test potential of –20 mV. Currents were leakage-subtracted. The dashed lines show the 0 current level. (c) The average steady-state current (Iss) is plotted as a function of the peak current (n = 4, hH1; n = 5, ΔΚ1500). (d and e) Single-channel currents recorded in cell-attached membrane patches with 200-ms pulses to a test potential of –20 mV with low-resistance microelectrodes. The upper four tracers in each panel show the responses to four consecutive trials. The lowest tracts show the average current. The dashed lines indicate the 0 current level.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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