Polymorphisms but not mutations of the KCNQ1 gene are associated with lone atrial fibrillation in the Chinese Han population. (Q55114202)

21 June 2018

title

Polymorphisms but not mutations of the KCNQ1 gene are associated with lone atrial fibrillation in the Chinese Han population. (English)

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21 June 2018

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Hui-min Chu

1

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21 June 2018

Ming-jun Feng

2

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21 June 2018

Yi-gang Li

3

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21 June 2018

Yi-xin Zhang

4

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21 June 2018

Ji-fang Ma

5

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21 June 2018

Bin He

6

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21 June 2018

Yi-bo Yu

7

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21 June 2018

Jing Liu

8

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21 June 2018

Xiao-min Chen

9

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21 June 2018

language of work or name

English

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publication date

18 April 2013

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21 June 2018

The Scientific World Journal

published in

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21 June 2018

volume

2013

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21 June 2018

page(s)

373454

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21 June 2018

Creative Commons Attribution 3.0 Unported

copyright license

start time

1 January 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

cites work

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1 reference

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Common variants in KCNN3 are associated with lone atrial fibrillation

22 June 2018

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Augmented potassium current is a shared phenotype for two genetic defects associated with familial atrial fibrillation

22 June 2018

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

22 June 2018

1 reference

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Comprehensive mutation scanning of LMNA in 268 patients with lone atrial fibrillation

22 June 2018

1 reference

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A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillation

22 June 2018

1 reference

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Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation.

22 June 2018

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Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation

22 June 2018

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A common polymorphism in SCN5A is associated with lone atrial fibrillation

22 June 2018

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The single nucleotide polymorphisms of I(Ks) potassium channel genes and their association with atrial fibrillation in a Chinese population

22 June 2018

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Potassium channel gene mutations rarely cause atrial fibrillation

22 June 2018

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Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation

22 June 2018

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

22 June 2018

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KCNQ1 gain-of-function mutation in familial atrial fibrillation

22 June 2018

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Incident stroke after discharge from the hospital with a diagnosis of atrial fibrillation.

22 June 2018

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

22 June 2018

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Left ventricular dysfunction due to atrial fibrillation in patients initially believed to have idiopathic dilated cardiomyopathy

22 June 2018

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Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han population

22 June 2018

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The single nucleotide polymorphisms of Kir3.4 gene and their correlation with lone paroxysmal atrial fibrillation in Chinese Han population.

13 August 2018

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KCNE3 mutation V17M identified in a patient with lone atrial fibrillation

13 August 2018

1 reference

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KCNQ1 mutation Q147R is associated with atrial fibrillation and prolonged QT interval

13 August 2018

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13 August 2018

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Analysis of minK and eNOS genes as candidate loci for predisposition to non-valvular atrial fibrillation

13 August 2018

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https://api.crossref.org/works/10.1155%2F2013%2F373454

Identification of NPPA variants associated with atrial fibrillation in a Chinese GeneID population

21 January 2018

1 reference

PubMed

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inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1155/2013/373454

1 reference

21 June 2018

PMC publication ID

3654283

1 reference

21 June 2018

PubMed publication ID

23710137

1 reference

21 June 2018