Short QT phenotype in a family with genetic variants in the KCNH2 and SLC4A3 genes - The role of prediction tools, whole exome sequencing and genetic cascade screening

18 March 2019 (10:05 - 10:55)
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Congress Presentation Part of: Moderated ePosters 8: channelopathies & cardiomyopathies Other Genetic Variants EHRA Premium Access EHRA 2019