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Genotype-phenotype correlation of novel KV7.1 mutations identified in patients with Long QT syndrome

Session: Genetic basis
Topic: Genetic aspects of arrhythmias
Speaker: Doctor M. Refaat (Beirut, LB)
Event: ESC Congress 2017

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Doctor Marwan Refaat

American University of Beirut AUB, Beirut (Lebanon)
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Identification of genetic etiology of malignant arrhythmia in dilated cardiomyopathy.

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Study of pharmacodynamic and pharmacokinetic-mediated genetic susceptibility to drug-induced arrhythmia and sudden cardiac death

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Risk and prognosis of mutations in different regions of the KCNQ1 gene.

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Novel RYR2 mutations causative for long QT syndromes

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High frequency of CACNA1C mutations among genotyped LQTS patients

Speaker: Assistant Professor S. Ohno (Suita, JP)

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Access the full session

Genetic basis

Speakers: Doctor M. Refaat, Doctor D. Wang, Miss M. Martinez Matilla, Doctor M. Cicerchia, Doctor M. Fukuyama...
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ESC Congress 2017

26 August - 30 August 2017

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