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Molecular mechanism of a new cardiac syndrome associated with a regulatory element deletion of chromosome 4q25

29 August 2020 (08:30 - 08:30)
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Congress Presentation Part of: Risk of Sudden Cardiac Death in Patient with Ion Channel Disorders Genetic Aspects of Arrhythmias ESC Premium Access ESC Congress 2020

About the speaker

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Ms Manon Baudic

Institute of Thorax, Nantes (France)

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Splice site mutation of LMNA causes severe dilated cardiomyopathy via strong dominant reduction of total lamin expression
Doctor K. Kato (Otsu, JP)
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Role of an extensive diagnostic work-up in the detection of concealed cardiomyopathies in athletes with premature ventricular complexes and implications for sports' eligibility assessment
Doctor P. Compagnucci (Ancona, IT)
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KCNQ1 V141M and Short QT Syndrome: Are we dealing with a different entity?
Doctor G. Garcia Ordonez (Guadalajara, MX)
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Risk of Sudden Cardiac Death in Patient with Ion Channel Disorders

The Event

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ESC Congress 2020

29 August 2020 08:30 CET

ESC 365 is supported by

novartis Explore sponsored resources

ESC 365 is supported by

novartis Explore sponsored resources