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Article

Ryanodine receptor mutations in arrhythmia: The continuing mystery of channel dysfunction.

FEBS letters - 17 May 2010

Thomas N Lowri, Maxwell Chloé, Mukherjee Saptarshi, Williams Alan J

Abstract excerpt

Mutations in RyR2 are causative of an inherited disorder which often results in sudden cardiac death. Dysfunctional channel behaviour has been the subject of many investigations varying from single channel analysis through to complex animal models. This review discusses recent advances in the fie...

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Share to Arrhythmias, Cardiac
Share to Mutation
Share to Phosphorylation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polymorphism, Genetic

Share to Ryanodine Receptor Calcium Release Channel

Share to Tachycardia, Ventricular

Source

Identifiers

PMID: 20132818
DOI: 10.1016/j.febslet.2010.01.057

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20132818-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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