Biophysical phenotypes of SCN5A mutations causing long QT and Brugada syndromes (Q40833166)

24 September 2017

title

Biophysical phenotypes of SCN5A mutations causing long QT and Brugada syndromes (English)

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24 September 2017

Baroudi G

1

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24 September 2017

Chahine M

series ordinal

2

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24 September 2017

language of work or name

English

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publication date

1 December 2000

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24 September 2017

number of pages

5

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based on heuristic

inferred from page(s)

published in

FEBS Letters

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24 September 2017

volume

487

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24 September 2017

issue

2

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24 September 2017

page(s)

224-228

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Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

24 September 2017

cites work

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Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome

21 January 2018

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Sudden death in patients and relatives with the syndrome of right bundle branch block, ST segment elevation in the precordial leads V(1)to V(3)and sudden death

21 January 2018

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Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

21 January 2018

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Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes

21 January 2018

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A single Na(+) channel mutation causing both long-QT and Brugada syndromes

21 January 2018

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SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

21 January 2018

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Ionic mechanisms responsible for the electrocardiographic phenotype of the Brugada syndrome are temperature dependent

21 January 2018

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Novel LQT-3 mutation affects Na+ channel activity through interactions between alpha- and beta1-subunits

21 January 2018

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Effects of flecainide in patients with new SCN5A mutation: mutation-specific therapy for long-QT syndrome?

21 January 2018

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SCN5A mutation (T1620M) causing Brugada syndrome exhibits different phenotypes when expressed in Xenopus oocytes and mammalian cells

21 January 2018

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Molecular mechanism for an inherited cardiac arrhythmia

21 January 2018

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Multiple mechanisms of Na+ channel--linked long-QT syndrome

21 January 2018

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Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na+ channel

21 January 2018

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Comparison of heterologously expressed human cardiac and skeletal muscle sodium channels

21 January 2018

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Enhanced Na(+) channel intermediate inactivation in Brugada syndrome

21 January 2018

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Rate dependence of action potential duration and refractoriness in canine ventricular endocardium differs from that of epicardium: role of the transient outward current.

21 January 2018

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Sodium channel functioning based on an octagonal structure model

21 January 2018

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Two distinct congenital arrhythmias evoked by a multidysfunctional Na(+) channel

21 January 2018

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A novel SCN5A mutation associated with idiopathic ventricular fibrillation without typical ECG findings of Brugada syndrome

7 January 2021

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inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0014-5793(00)02360-7

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24 September 2017

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