Clinical, genetic and functional analysis of R562S-Kv7.1 mutation associated with long QT syndrome type 1

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Clinical, genetic and functional analysis of R562S-Kv7.1 mutation associated with long QT syndrome type 1

Session: Oral abstract session - WGCCE

Topic: Arrhythmias

Speaker: Doctor O. Svecova (Brno, CZ)

Event: EHRA 2021

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Doctor Olga Svecova

Masaryk University, Brno (Czechia)

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Oral abstract session - WGCCE

Speakers: Doctor O. Svecova, Ms L. Sommerfeld, Mr M. Sadredini, Doctor M. O'Reilly, Mr A. Wagdi Mohamed...

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EHRA 2021

23 April - 25 April 2021

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