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JPH2 p.(Thr161Lys) is a Finnish founder mutation associating to hypertrophic cardiomyopathy with or without systolic heart failure and conduction abnormalities

28 August 2018 (14:00 - 18:00)
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Congress Presentation Part of: Poster Session 7 - Genetics in cardiomyopathies Hypertrophic Cardiomyopathy ESC Premium Access ESC Congress 2018

About the speaker

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Doctor Juha Koskenvuo

Turku University Hospital, Turku (Finland)

13 More presentations in this session

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Doctor J. Ochoa (A Coruna, ES)
Abstract Slides
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Miss E. Field (London, GB)
Abstract Slides
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Doctor T. Robyns (Leuven, BE)
Abstract
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Associate Professor J. Bonaventura (Prague, CZ)
Abstract
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Doctor K. Nguyen (Marseille, FR)
Abstract Slides

Access the full session

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Poster Session 7 - Genetics in cardiomyopathies

The Event

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ESC Congress 2018

28 August 2018 14:00 CET

ESC 365 is supported by

novartis Explore sponsored resources

ESC 365 is supported by

novartis Explore sponsored resources