(Q48549245)

12 February 2018

title

SCN5A mutation associated with cardiac conduction defect and atrial arrhythmias. (English)

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12 February 2018

author name string

Päivi J Laitinen-Forsblom

1

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12 February 2018

Pekka Mäkynen

2

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12 February 2018

Heikki Mäkynen

3

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12 February 2018

Sinikka Yli-Mäyry

4

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12 February 2018

Vesa Virtanen

5

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12 February 2018

Kimmo Kontula

6

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12 February 2018

Katriina Aalto-Setälä

7

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12 February 2018

publication date

1 May 2006

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12 February 2018

Journal of Cardiovascular Electrophysiology

published in

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12 February 2018

volume

17

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12 February 2018

page(s)

480-485

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12 February 2018

issue

5

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12 February 2018

Chronic Bifascicular Block: Evaluation of Familial Factors

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1 reference

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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

21 January 2018

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Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease

21 January 2018

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Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)

21 January 2018

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Cardiac conduction defects associate with mutations in SCN5A

21 January 2018

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A sodium-channel mutation causes isolated cardiac conduction disease

21 January 2018

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Cardiac sodium channel and inherited arrhythmia syndromes

21 January 2018

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Molecular mechanism for an inherited cardiac arrhythmia

21 January 2018

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Cardiac Sodium Channel Diseases

21 January 2018

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

21 January 2018

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Flecainide test in Brugada syndrome: a reproducible but risky tool.

21 January 2018

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Rapid platelet-function assay: an automated and quantitative cartridge-based method

21 January 2018

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

21 January 2018

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SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia

21 January 2018

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Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

21 January 2018

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Brugada syndrome and supraventricular tachyarrhythmias: a novel association?

21 January 2018

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A reinterpretation of mammalian sodium channel gating based on single channel recording

21 January 2018

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21 January 2018

Identifiers

DOI

1 reference

12 February 2018

PubMed ID

16684018

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12 February 2018