A novel SCN5A mutation associated with long QT-3: altered inactivation kinetics and channel dysfunction. (Q33148068)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12209021%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

title

A novel SCN5A mutation associated with long QT-3: altered inactivation kinetics and channel dysfunction (English)

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12 November 2019

3

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12 November 2019

author name string

Ilaria Rivolta

1

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12 November 2019

Colleen E Clancy

2

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12 November 2019

Huajun Liu

4

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12 November 2019

Silvia G Priori

5

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12 November 2019

Robert S Kass

6

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12 November 2019

publication date

3 September 2002

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12 November 2019

published in

Physiological Genomics

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12 November 2019

volume

10

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12 November 2019

issue

3

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12 November 2019

page(s)

191-197

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Novel arrhythmogenic mechanism revealed by a long-QT syndrome mutation in the cardiac Na(+) channel.

12 November 2019

cites work

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

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Na(+) channel mutation that causes both Brugada and long-QT syndrome phenotypes: a simulation study of mechanism

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21 January 2018

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Phenotypic characterization of a novel long-QT syndrome mutation (R1623Q) in the cardiac sodium channel

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Role of the C-terminal domain in inactivation of brain and cardiac sodium channels

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21 January 2018

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Subconductance states of a mutant NMDA receptor channel kinetics, calcium, and voltage dependence

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Estimating single-channel kinetic parameters from idealized patch-clamp data containing missed events

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Inherited long QT syndromes: a paradigm for understanding arrhythmogenesis

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A Met-to-Val mutation in the skeletal muscle Na+ channel alpha-subunit in hyperkalaemic periodic paralysis

21 January 2018

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Cardiac conduction defects associate with mutations in SCN5A

21 January 2018

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Characterization of human cardiac Na+ channel mutations in the congenital long QT syndrome

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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De novo mutation in the SCN5A gene associated with early onset of sudden infant death

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