(Q44700554)

5 December 2017

title

A cardiac sodium channel mutation identified in Brugada syndrome associated with atrial standstill (English)

1 reference

5 December 2017

1 reference

Takehara N

1 reference

5 December 2017

Makita N

1 reference

5 December 2017

Kawabe J

1 reference

5 December 2017

Sato N

1 reference

5 December 2017

Kawamura Y

1 reference

5 December 2017

Kitabatake A

1 reference

5 December 2017

Kikuchi K

1 reference

5 December 2017

language of work or name

English

0 references

publication date

1 January 2004

1 reference

Journal of Internal Medicine

5 December 2017

published in

1 reference

5 December 2017

volume

255

1 reference

5 December 2017

1 reference

5 December 2017

page(s)

137-142

1 reference

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

5 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01247.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01247.X

Cardiac conduction defects associate with mutations in SCN5A

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01247.X

A sodium-channel mutation causes isolated cardiac conduction disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01247.X

Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01247.X

Clinical, genetic, and biophysical characterization of SCN5A mutations associated with atrioventricular conduction block

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01247.X

A novel SCN5A arrhythmia mutation, M1766L, with expression defect rescued by mexiletine

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01247.X

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01247.X

Sodium channel blockers identify risk for sudden death in patients with ST-segment elevation and right bundle branch block but structurally normal hearts

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01247.X

A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01247.X

Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01247.X

Drug-induced long-QT syndrome associated with a subclinical SCN5A mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01247.X

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01247.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01247.X

A mutant cardiac sodium channel with multiple biophysical defects associated with overlapping clinical features of Brugada syndrome and cardiac conduction disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01247.X

Genomic organization of the human SCN5A gene encoding the cardiac sodium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01247.X

The Brugada syndrome: diagnostic criteria and cellular mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01247.X

10.1046/J.0954-6820.2003.01247.X

21 January 2018

Identifiers

DOI

1 reference

5 December 2017

1 reference