(Q31119456)

29 June 2017

A common human SCN5A polymorphism modifies expression of an arrhythmia causing mutation (English)

1 reference

29 June 2017

0 references

3

Michael J Ackerman

1 reference

29 June 2017

Bin Ye

1

1 reference

PubMed ID

12454206

29 June 2017

Carmen R Valdivia

series ordinal

2

1 reference

PubMed ID

12454206

29 June 2017

Jonathan C Makielski

series ordinal

4

1 reference

29 June 2017

6 February 2003

1 reference

29 June 2017

Physiological Genomics

1 reference

29 June 2017

12

1 reference

29 June 2017

187-193

1 reference

29 June 2017

3

1 reference

Novel arrhythmogenic mechanism revealed by a long-QT syndrome mutation in the cardiac Na(+) channel.

29 June 2017

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00117.2002

Ion channels--basic science and clinical disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00117.2002

Expression and intracellular localization of an SCN5A double mutant R1232W/T1620M implicated in Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00117.2002

Novel mechanism for Brugada syndrome: defective surface localization of an SCN5A mutant (R1432G).

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00117.2002

A single Na(+) channel mutation causing both long-QT and Brugada syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00117.2002

Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00117.2002

Nomenclature of voltage-gated sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00117.2002

Effects of III-IV linker mutations on human heart Na+ channel inactivation gating

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00117.2002

Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00117.2002

Molecular and cellular mechanisms of cardiac arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00117.2002

Rate-dependent QT shortening mechanism for the LQT3 deltaKPQ mutant

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00117.2002

Arrhythmogenic mechanism of an LQT-3 mutation of the human heart Na(+) channel alpha-subunit: A computational analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00117.2002

Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00117.2002

Mechanisms for intragenic complementation at the human argininosuccinate lyase locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00117.2002

Linking a genetic defect to its cellular phenotype in a cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00117.2002

10.1152/PHYSIOLGENOMICS.00117.2002

21 January 2018

Identifiers

DOI

1 reference

29 June 2017

1 reference

PubMed ID

12454206