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Complex inherited cardiac diseases inheritance in a family harbouring compound SCN5A and MYBPC3 mutations.

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About the speaker

Doctor Ruggiero Mango

University of Rome Tor Vergata, Rome (Italy)
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28 more presentations in this session

A novel CACNA1C mutation identified in a patient with atypical Timothy syndrome exerts both loss- and gain-of-function effects on Cav1.2.

Speaker: Doctor J. Ozawa (Niigata, JP)

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Genetic testing in a consecutive series of young athletes with suspected cathecolaminargic polymorphic ventricular tachycardia

Speaker: Associate Professor N. Marziliano (Milan, IT)

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The burden of complex arrhythmic genotypes in a consecutive series of Sardinian population of patients with primary arrhythmic disorders

Speaker: Associate Professor N. Marziliano (Milan, IT)

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Discrepancy of QTc duration and LQTS risk score for the diagnosis of type 3 LQTS

Speaker: Doctor A. Hermida (Paris, FR)

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Triple mutations in three major genes for long QT syndrome are very rare and cause complicated phenotypes with ventricular arrhythmia

Speaker: Doctor S. Ohno (Suita, JP)

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Poster session 4 - Miscellaneous in arrhythmia

Speakers: Doctor R. Mango, Doctor J. Ozawa, Associate Professor N. Marziliano, Associate Professor N. Marziliano, Doctor A. Hermida...
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ESC CONGRESS 2016

27 August - 31 August 2016

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