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Doctor Elena Zaklyazminskaya

Petrovsky National Research Center of Surgery, Moscow (Russian Federation)

Presentations

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

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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?

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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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