Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts (Q33145152)

22 July 2017

Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts (English)

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22 July 2017

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ventricular tachycardia

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7

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22 July 2017

Swan H

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22 July 2017

Piippo K

2

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22 July 2017

Viitasalo M

3

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22 July 2017

Heikkilä P

4

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22 July 2017

Paavonen T

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22 July 2017

Kainulainen K

6

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22 July 2017

Keto P

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22 July 2017

Kontula K

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22 July 2017

Toivonen L

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22 July 2017

language of work or name

English

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publication date

1 December 1999

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Journal of the American College of Cardiology

22 July 2017

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22 July 2017

34

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22 July 2017

2035-2042

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22 July 2017

7

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The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome

22 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Right ventricular cardiomyopathy and sudden death in young people

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https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy

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https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

The molecular genetics of the long QT syndrome: genes causing fainting and sudden death

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: a multicenter study.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

A new locus for arrhythmogenic right ventricular cardiomyopathy (ARVD2) maps to chromosome 1q42-q43

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https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm

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https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

The gene for arrhythmogenic right ventricular cardiomyopathy maps to chromosome 14q23-q24

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https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

A new locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23.

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https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Ventricular activation during ventricular endocardial pacing: I. Electrocardiographic patterns related to the site of pacing

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https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Use of signals in the terminal QRS complex to identify patients with ventricular tachycardia after myocardial infarction

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Diagnostic accuracy of right ventriculography in arrhythmogenic right ventricular cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Right ventricular performance in patients with coronary artery disease

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https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

A metric map of humans: 23,500 loci in 850 bands

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

TWIK-1, a ubiquitous human weakly inward rectifying K+ channel with a novel structure

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Molecular cloning and sequence analysis of human genomic DNA encoding a novel membrane protein which exhibits a slowly activating potassium channel activity

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Cloning of a membrane protein that induces a slow voltage-gated potassium current

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Assignment of the human weak inward rectifier K+ channel TWIK-1 gene to chromosome 1q42-q43.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

The molecular genetics of hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23.

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https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)

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https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Task Force of the Working Group Myocardial and Pericardial Disease of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the International S

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Arrhythmogenic right ventricular cardiomyopathy and fatty replacement of the right ventricular myocardium: are they different diseases?

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Evidence of Apoptosis in Arrhythmogenic Right Ventricular Dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Value of quantitative measurement of signal-averaged electrocardiographic variables in arrhythmogenic right ventricular dysplasia: correlation with echocardiographic right ventricular cavity dimensions

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Juvenile sudden death and effort ventricular tachycardias in a family with right ventricular cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Bidirectional tachycardia in a child. A study using His bundle electrography

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

The human cardiac muscle ryanodine receptor-calcium release channel: identification, primary structure and topological analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900461-1

7 January 2021

10.1016/S0735-1097(99)00461-1

Identifiers

DOI

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22 July 2017

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