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Novel RYR2 mutations causative for long QT syndromes

29 August 2017 (15:35 - 16:25)
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Congress Presentation Part of: Genetic basis Genetic aspects of arrhythmias ESC Premium Access ESC Congress 2017

About the speaker

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Doctor Megumi Fukuyama

Shiga University of Medical Science, Otsu (Japan)

6 More presentations in this session

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Identification of genetic etiology of malignant arrhythmia in dilated cardiomyopathy.
Doctor D. Wang (Nanjing, CN)
Abstract
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Study of pharmacodynamic and pharmacokinetic-mediated genetic susceptibility to drug-induced arrhythmia and sudden cardiac death
Miss M. Martinez Matilla (Santiago de Compostela, ES)
Abstract Slides
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Risk and prognosis of mutations in different regions of the KCNQ1 gene.
Doctor M. Cicerchia (Espoo, FI)
Abstract Slides
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Genotype-phenotype correlation of novel KV7.1 mutations identified in patients with Long QT syndrome
Doctor M. Refaat (Beirut, LB)
Abstract Slides
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High frequency of CACNA1C mutations among genotyped LQTS patients
Assistant Professor S. Ohno (Suita, JP)
Abstract Slides

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Genetic basis

The Event

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ESC Congress 2017

29 August 2017 15:35 CET
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