(Q36118504)

12 August 2017

1 reference

title

Is atrial fibrillation a genetic disease? (English)

1 reference

12 August 2017

1 reference

1

Ramon Brugada

1 reference

12 August 2017

1 May 2005

1 reference

Journal of Cardiovascular Electrophysiology

12 August 2017

1 reference

12 August 2017

16

1 reference

12 August 2017

5

1 reference

12 August 2017

553-556

1 reference

Atrial fibrillation: a major contributor to stroke in the elderly. The Framingham Study

12 August 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40703.X

Presentation and management of patients admitted with atrial fibrillation: a review of 291 cases in a regional hospital

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40703.X

Parental atrial fibrillation as a risk factor for atrial fibrillation in offspring

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40703.X

Familial atrial fibrillation is a genetically heterogeneous disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40703.X

Identification of a genetic locus for familial atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40703.X

KCNQ1 gain-of-function mutation in familial atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40703.X

Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40703.X

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40703.X

Sudden death associated with short-QT syndrome linked to mutations in HERG.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40703.X

Renin-angiotensin system gene polymorphisms and atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40703.X

Association of the human minK gene 38G allele with atrial fibrillation: evidence of possible genetic control on the pathogenesis of atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40703.X

Relation of the -174 G/C polymorphism of interleukin-6 to interleukin-6 plasma levels and to length of hospitalization after surgical coronary revascularization

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40703.X

Compound mutations: a common cause of severe long-QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.40703.X

10.1111/J.1540-8167.2005.40703.X

21 January 2018

Identifiers

DOI

1 reference

12 August 2017

1 reference

PubMed ID

15877629