Cardiac channelopathies: it's in the genes. (Q47662421)

4 February 2018

title

Cardiac channelopathies: it's in the genes. (English)

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4 February 2018

author name string

Michael J Ackerman

series ordinal

1

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4 February 2018

language of work or name

English

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publication date

1 May 2004

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4 February 2018

published in

Nature Medicine

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4 February 2018

volume

10

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4 February 2018

issue

5

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4 February 2018

page(s)

463-464

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4 February 2018

https://scigraph.springernature.com/pub.10.1038/nm0504-463

exact match

0 references

cites work

Ion channels--basic science and clinical disease

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A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

21 January 2018

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SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

21 January 2018

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A family of potassium channel genes related to eag in Drosophila and mammals

21 January 2018

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A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel

21 January 2018

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Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

21 January 2018

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Molecular basis of the long-QT syndrome associated with deafness.

21 January 2018

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The long QT syndrome: a prospective international study

21 January 2018

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Mutations in the hminK gene cause long QT syndrome and suppress IKs function

21 January 2018

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MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

21 January 2018

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Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

21 January 2018

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KCNQ1 gain-of-function mutation in familial atrial fibrillation

21 January 2018

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Sudden death associated with short-QT syndrome linked to mutations in HERG.

21 January 2018

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Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

21 January 2018

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Cardiac conduction defects associate with mutations in SCN5A

21 January 2018

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Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

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Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome.

21 January 2018

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

21 January 2018

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Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

21 January 2018

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Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.

21 January 2018

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Effectiveness and limitations of beta-blocker therapy in congenital long-QT syndrome.

21 January 2018

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Risk stratification in the long-QT syndrome.

21 January 2018

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Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene

21 January 2018

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inferred from DOI database lookup

7 January 2021

based on heuristic

ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNM0504-463

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NM0504-463

1 reference

4 February 2018

PubMed ID

15122246

1 reference

4 February 2018