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Cited by 296

The DOI matches its Crossref record; 61 of the 61 references it cites were found in a registry or an index.

Long QT syndrome: from channels to cardiac arrhythmias

Open access
Moss, A. J.·2005·Journal of Clinical Investigation

Abstract

Long QT syndrome, a rare genetic disorder associated with life-threatening arrhythmias, has provided a wealth of information about fundamental mechanisms underlying human cardiac electrophysiology that has come about because of truly collaborative interactions between clinical and basic scientists. Our understanding of the mechanisms that control the critical plateau and repolarization phases of the human ventricular action potential has been raised to new levels through these studies, which have clarified the manner in which both potassium and sodium channels regulate this critical period of electrical activity.

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Metadata

Authors
Moss, A. J.
Venue
Journal of Clinical Investigation
Published
2005-08-01
Volume
115
Issue
8
Pages
2018-2024
ISSN
0021-9738 (ISSN-L)
OpenAlex
W2074519955
Cited by
296
References
61
FWCI
12.73
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Long QT syndrome: from channels to cardiac arrhythmias. https://app.cochat.ai/papers/10.1172/jci25537
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Moss, A. J. (2005). Long QT syndrome: from channels to cardiac arrhythmias. Journal of Clinical Investigation. https://doi.org/10.1172/jci25537

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.