Prominent QTc prolongation in a patient with a rare variant in the cardiac ryanodine receptor gene. - Wikidata - awgldk - TriplyDB

Prominent QTc prolongation in a patient with a rare variant in the cardiac ryanodine receptor gene.

Prominent QTc prolongation in a patient with a rare variant in the cardiac ryanodine receptor gene.

http://www.wikidata.org/entity/Q33167409

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Bradycardia is a Specific Phenotype of Catecholaminergic Polymorphic Ventricular Tachycardia Induced by RYR2 Mutations.

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Prominent QTc prolongation in a patient with a rare variant in the cardiac ryanodine receptor gene.

http://www.wikidata.org/entity/Q33167409

description

2016 nî lūn-bûn

@nan

2016 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2016 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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Heart and Vessels

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@en

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Aya Miyazaki

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Heima Sakaguchi

http://www.w3.org/2001/XMLSchema#string

Hideo Ohuchi

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Jun Negishi

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Kanae Noritake

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Norihiro Ebishima

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Takeshi Aiba

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Wataru Shimizu

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Yoshihiro Miyamoto

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Yousuke Hayama

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P2860

The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading fram

Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes

Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia.

A novel cardiac ryanodine receptor gene (RyR2) mutation in an athlete with aborted sudden cardiac death: a case of adult-onset catecholaminergic polymorphic ventricular tachycardia.

Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testing.

Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromes.

The long QT syndrome and catecholaminergic polymorphic ventricular tachycardia.

Current perspectives in genetic cardiovascular disorders: from basic to clinical aspects.

HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013.

Diagnostic value of epinephrine test for genotyping LQT1, LQT2, and LQT3 forms of congenital long QT syndrome.

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229-233

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