(Q34179377)

31 July 2017

High prevalence of genetic variants previously associated with LQT syndrome in new exome data (English)

1 reference

31 July 2017

Lena Refsgaard

1

0 references

Morten Salling Olesen

object named as

Morten S Olesen

6

0 references

Anders G Holst

object named as

Anders G Holst

2

0 references

Stig Haunsø

4

object named as

Stig Haunsø

1 reference

31 July 2017

Golnaz Sadjadieh

3

1 reference

PubMed ID

22378279

31 July 2017

Jonas B Nielsen

5

1 reference

31 July 2017

29 February 2012

1 reference

European Journal of Human Genetics

31 July 2017

1 reference

31 July 2017

20

1 reference

31 July 2017

8

1 reference

31 July 2017

905-908

1 reference

Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported

31 July 2017

start time

29 February 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

exact match

https://scigraph.springernature.com/pub.10.1038/ejhg.2012.23

0 references

cites work

A novel nonsense variant in Nav1.5 cofactor MOG1 eliminates its sodium current increasing effect and may increase the risk of arrhythmias

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400735

Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400735

Identification of a Kir3.4 mutation in congenital long QT syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400735

Epidemiologic, molecular, and functional evidence suggest A572D-SCN5A should not be considered an independent LQT3-susceptibility mutation.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400735

A method and server for predicting damaging missense mutations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400735

The genetic basis of long QT and short QT syndromes: a mutation update

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400735

5 July 2018

Identifiers

DOI

10.1038/EJHG.2012.23

1 reference

31 July 2017

1 reference

31 July 2017

1 reference

PubMed ID

22378279