Novel connexin40 missense mutations in patients with familial atrial fibrillation (Q44343773)

2 December 2017

title

Novel connexin40 missense mutations in patients with familial atrial fibrillation (English)

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2 December 2017

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Yi-Qing Yang

1

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2 December 2017

Xu Liu

2

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2 December 2017

Xian-Ling Zhang

3

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2 December 2017

Xin-Hua Wang

4

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2 December 2017

Hong-Wei Tan

5

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2 December 2017

Hai-Feng Shi

6

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2 December 2017

Wei-Feng Jiang

7

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2 December 2017

Wei-Yi Fang

8

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2 December 2017

publication date

21 July 2010

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2 December 2017

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2 December 2017

volume

12

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2 December 2017

issue

10

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2 December 2017

page(s)

1421-1427

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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

2 December 2017

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A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

21 January 2018

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Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry

21 January 2018

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Common variants in KCNN3 are associated with lone atrial fibrillation

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Identification of a genetic locus for familial atrial fibrillation

21 January 2018

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Genome-wide linkage scan identifies a novel genetic locus on chromosome 5p13 for neonatal atrial fibrillation associated with sudden death and variable cardiomyopathy

21 January 2018

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KCNQ1 gain-of-function mutation in familial atrial fibrillation

21 January 2018

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Atrial fibrillation is associated with accumulation of aging-related common type mitochondrial DNA deletion mutation in human atrial tissue.

21 January 2018

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

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

21 January 2018

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Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation

21 January 2018

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Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac death

21 January 2018

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21 January 2018

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21 January 2018

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Conduction disturbances and increased atrial vulnerability in Connexin40-deficient mice analyzed by transesophageal stimulation.

21 January 2018

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Gap junctional remodeling in relation to stabilization of atrial fibrillation in the goat

21 January 2018

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Gap junction alterations in human cardiac disease.

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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Prolonged signal-averaged P-wave duration as an intermediate phenotype for familial atrial fibrillation

21 January 2018

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21 January 2018

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The role of connexin40 in atrial fibrillation

21 January 2018

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Altered right atrial excitation and propagation in connexin40 knockout mice

21 January 2018

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The gap junction modifier, GAP-134 [(2S,4R)-1-(2-aminoacetyl)-4-benzamido-pyrrolidine-2-carboxylic acid], improves conduction and reduces atrial fibrillation/flutter in the canine sterile pericarditis model.

21 January 2018

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Effects of selective vagal and stellate ganglion stimulation of atrial refractoriness.

21 January 2018

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21 January 2018

Identifiers

DOI

10.1093/EUROPACE/EUQ274

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2 December 2017

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