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Article

Recurrent ventricular fibrillation in a young female carrying a previously unidentified RyR2 gene mutation.

International journal of cardiology - 15 Dec 2015

Kron Jordana, Ellenbogen Kenneth, Abbate Antonio

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Share to Adolescent
Share to Defibrillators, Implantable
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Ryanodine Receptor Calcium Release Channel

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Source

Identifiers

PMID: 26298385
DOI: 10.1016/j.ijcard.2015.08.044

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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Recurrent ventricular fibrillation in a young female carrying a previously unidentified RyR2 gene mutation.PMID 26298385Read ↗

A novel RyR2 mutation in a 2-year-old baby presenting with atrial fibrillation, atrial flutter, and atrial ectopic tachycardia.Semantic proximity Read ↗

Ryanodine receptor mutations presenting as idiopathic ventricular fibrillation: a report on two novel familial compound mutations, c.6224T>C and c.13781A>G, with the clinical presentation of idiopathic ventricular fibrillation.Semantic proximity Read ↗

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Rare RYR2 p.Thr85Ile variant is associated with catecholaminergic polymorphic ventricular tachycardia.Semantic proximity Read ↗

A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia.Semantic proximity Read ↗

Classification and correlation of RYR2 missense variants in individuals with catecholaminergic polymorphic ventricular tachycardia reveals phenotypic relationships.Semantic proximity Read ↗

Cardiac ryanodine receptor gene (hRyR2) mutation underlying catecholaminergic polymorphic ventricular tachycardia in a Chinese adolescent presenting with sudden cardiac arrest and cardiac syncope.Semantic proximity Read ↗

Prognosis and clinical management of asymptomatic family members with RYR2-mediated catecholaminergic polymorphic ventricular tachycardia: a review.Semantic proximity Read ↗

Non-ventricular, Clinical, and Functional Features of the RyR2(R420Q) Mutation Causing Catecholaminergic Polymorphic Ventricular Tachycardia.Semantic proximity Read ↗

An RyR2 mutation found in a family with a short-coupled variant of torsade de pointes.Semantic proximity Read ↗

Cardiac Arrest in a Young Woman: A Near Miss Diagnosis.Semantic proximity Read ↗

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