Sodium channel mutations and susceptibility to heart failure and atrial fibrillation (Q28304352)

2

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Jeffrey D Ballew

3

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Sandra P Reyna

4

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Margaret L Karst

5

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Kathleen J Herron

6

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Steven C Horton

7

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Richard J Rodeheffer

8

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Jeffrey L Anderson

The Journal of the American Medical Association

9

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language of work or name

English

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publication date

26 January 2005

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published in

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volume

293

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issue

4

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page(s)

447-54

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cites work

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Many roads lead to a broken heart: the genetics of dilated cardiomyopathy

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Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy

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Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

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Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

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Cardiac conduction defects associate with mutations in SCN5A

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Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

20 March 2017

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Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

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Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

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Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutations

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Slowed conduction and ventricular tachycardia after targeted disruption of the cardiac sodium channel gene Scn5a

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Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban

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Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system

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SNP S1103Y in the cardiac sodium channel gene SCN5A is associated with cardiac arrhythmias and sudden death in a white family

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

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Na+ channel activators as positive inotropic agents for the treatment of chronic heart failure

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

29 September 2017

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Metavinculin mutations alter actin interaction in dilated cardiomyopathy.

27 November 2018

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

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12 December 2020

Natural history of dilated cardiomyopathy due to lamin A/C gene mutations

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12 December 2020

Sodium and the heart: a hidden key factor in cardiac regulation

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12 December 2020

Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975-1984

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X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus

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12 December 2020

Identifiers

DOI

10.1001/JAMA.293.4.447

1 reference

1 reference

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PubMed publication ID

15671429

1 reference