(Q37099702)

18 August 2017

1 reference

title

Genetics of atrial fibrillation: rare mutations, common polymorphisms, and clinical relevance (English)

1 reference

18 August 2017

0 references

Dawood Darbar

1

1 reference

18 August 2017

18 September 2007

1 reference

18 August 2017

1 reference

18 August 2017

5

1 reference

18 August 2017

483-486

1 reference

18 August 2017

3

1 reference

Genomewide association analysis of coronary artery disease

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2292402

Variants conferring risk of atrial fibrillation on chromosome 4q25.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2292402

Polymorphism modulates symptomatic response to antiarrhythmic drug therapy in patients with lone atrial fibrillation

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2292402

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

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2292402

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

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2292402

Atrial fibrillation in KCNE1-null mice

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2292402

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

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2292402

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

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2292402

Renin-angiotensin system gene polymorphisms and atrial fibrillation

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2292402

Familial atrial fibrillation is a genetically heterogeneous disorder.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2292402

KCNQ1 gain-of-function mutation in familial atrial fibrillation

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2292402

Familial aggregation of atrial fibrillation in Iceland

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2292402

Atrial fibrillation-associated minK38G/S polymorphism modulates delayed rectifier current and membrane localization.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2292402

Human atrial ion channel and transporter subunit gene-expression remodeling associated with valvular heart disease and atrial fibrillation.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2292402

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

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2292402

Familial aggregation in lone atrial fibrillation

3 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18313611

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Stretch-sensitive KCNQ1 mutation A link between genetic and environmental factors in the pathogenesis of atrial fibrillation?

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18313611

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.HRTHM.2007.09.002

1 reference

18 August 2017

1 reference

18 August 2017

1 reference

PMCID

2292402