Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease (Q61773863)

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31 October 2019

title

Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease (English)

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31 October 2019

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1

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31 October 2019

Florence Kyndt

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31 October 2019

Jean-Jacques Schott

7

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31 October 2019

Isabelle Baró

8

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31 October 2019

author name string

Franck Potet

3

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31 October 2019

Jean-Noel Trochu

4

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31 October 2019

Guy Mialet

5

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31 October 2019

Sophie Demolombe

6

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31 October 2019

Denis Escande

9

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31 October 2019

Hervé Le Marec

10

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31 October 2019

language of work or name

English

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publication date

1 February 2003

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Journal of the American College of Cardiology

31 October 2019

published in

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31 October 2019

volume

41

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31 October 2019

issue

4

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31 October 2019

page(s)

643-652

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Chronic Bifascicular Block: Evaluation of Familial Factors

31 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

A survey of familial heart block

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

Four cases of benign left bundle branch block in the same family

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

Familial bundle branch block

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

Familial trifascicular block

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

Familial fascicular block: histologic features of Lev's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

Gene for progressive familial heart block type I maps to chromosome 19q13.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

Cardiac conduction defects associate with mutations in SCN5A

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

Calculating confidence intervals for regression and correlation.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

Molecular biology of sodium channels and their role in cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

Modulation of cardiac Na+ current phenotype by beta1-subunit expression

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

A histological study of the conduction system in complete heart block

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

Genetic manipulation of cardiac K(+) channel function in mice: what have we learned, and where do we go from here?

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

Cardiac sodium channel and inherited arrhythmia syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patients

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

Clinical and molecular heterogeneity in the Brugada syndrome: a novel gene locus on chromosome 3.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2902864-4

7 January 2021

10.1016/S0735-1097(02)02864-4

Identifiers

DOI

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31 October 2019

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