Doctor Elena Zaklyazminskaya
Petrovsky National Research Center of Surgery, Moscow (Russian Federation)
Expanding the phenotype of loss-of-function mutations in the PPP1R13L gene causing paediatric dilated cardiomyopathy
Event: Heart Failure 2019
Topic: Cardiomyopathies
Session: Basic Science
De novo mutation rate in patients with hypertrophic cardiomyopathy and left ventricular non-compaction.
Event: Heart Failure 2018
Topic: Genetics, Epigenetics, ncRNA
Session: Comorbidities and cardiomyopathies - How to manage?
New insight into the clinical polymorphism of SCNA-related arrhythmic syndromes revealed by deep phenotyping
Event: EHRA EUROPACE - CARDIOSTIM 2017
Topic: Genetics (Basic Science in Arrhythmias)
Session: Late Breaking Science - Poster Session
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