Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation-Reference-Cited by-同舟云学术

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Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation

Published:2009-08 Issue:8 Volume:6 Page:1146-1153
ISSN:1547-5271
Container-title:Heart Rhythm
language:en
Short-container-title:Heart Rhythm

Author:

Das Saumya,Makino Seiko,Melman Yonathan F.,Shea Marisa A.,Goyal Sanjeev B.,Rosenzweig Anthony,MacRae Calum A.,Ellinor Patrick T.

Publisher

Elsevier BV

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference21 articles.

1. Prevalence of diagnosed atrial fibrillation in adults: national implications for rhythm management and stroke prevention: the AnTicoagulation and Risk Factors in Atrial Fibrillation (ATRIA) Study;Go;JAMA,2001

2. Temporal relations of atrial fibrillation and congestive heart failure and their joint influence on mortality: the Framingham Heart Study;Wang;Circulation,2003

3. Parental atrial fibrillation as a risk factor for atrial fibrillation in offspring;Fox;JAMA,2004

4. Familial aggregation in lone atrial fibrillation;Ellinor;Hum Genet,2005

5. Identification of a genetic locus for familial atrial fibrillation;Brugada;N Engl J Med,1997

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1. Genetic Atrial Fibrillation;Reference Module in Biomedical Sciences;2024

2. Mutation-Specific Differences in Kv7.1 (KCNQ1) and Kv11.1 (KCNH2) Channel Dysfunction and Long QT Syndrome Phenotypes;International Journal of Molecular Sciences;2022-07-02

3. Genetic and non-genetic risk factors associated with atrial fibrillation;Life Sciences;2022-06

4. Genetically based atrial fibrillation: Current considerations for diagnosis and management;Journal of Cardiovascular Electrophysiology;2022-03-19

5. Inherited and Acquired Rhythm Disturbances in Sick Sinus Syndrome, Brugada Syndrome, and Atrial Fibrillation: Lessons from Preclinical Modeling;Cells;2021-11-15

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