(Q33252748)

24 July 2017

Potassium channel gene mutations rarely cause atrial fibrillation (English)

1 reference

24 July 2017

0 references

1

Patrick T Ellinor

1 reference

24 July 2017

Vadim I Petrov-Kondratov

2

1 reference

24 July 2017

Elena Zakharova

3

1 reference

24 July 2017

Edwin G Nam

4

1 reference

24 July 2017

Calum A MacRae

5

1 reference

24 July 2017

3 August 2006

1 reference

24 July 2017

1 reference

24 July 2017

7

1 reference

24 July 2017

70

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2350-7-70

24 July 2017

0 references

cites work

Ménière's disease is associated with single nucleotide polymorphisms in the human potassium channel genes, KCNE1 and KCNE3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559598

A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559598

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559598

Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559598

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559598

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559598

Familial atrial fibrillation is a genetically heterogeneous disorder.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559598

KCNQ1 gain-of-function mutation in familial atrial fibrillation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559598

New ideas about atrial fibrillation 50 years on.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559598

Epidemiology and natural history of atrial fibrillation: clinical implications

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559598

Impact of atrial fibrillation on the risk of death: the Framingham Heart Study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559598

Identification of a genetic locus for familial atrial fibrillation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559598

Polymorphism of the gene encoding a human minimal potassium ion channel (minK)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559598

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559598

De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero.

21 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-70

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-70

[Thyrotoxic hypokalemic periodic paralysis, an endocrine emergency: clinical and genetic features in 25 patients].

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-70

DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-70

Locus for atrial fibrillation maps to chromosome 6q14-16

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16887036

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The efficacy of quinidine and disopyramide in the maintenance of sinus rhythm after electroconversion from atrial fibrillation. A double-blind study comparing quinidine, disopyramide and placebo

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16887036

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16887036

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2350-7-70

1 reference

Dimensions Publication ID

24 July 2017

0 references

1 reference

24 July 2017

1 reference