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Doctor Elena Zaklyazminskaya

Petrovsky National Research Center of Surgery, Moscow (Russian Federation)
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Expanding the phenotype of loss-of-function mutations in the PPP1R13L gene causing paediatric dilated cardiomyopathy
Presentation
Expanding the phenotype of loss-of-function mutations in the PPP1R13L gene causing paediatric dilated cardiomyopathy
De novo mutation rate in patients with hypertrophic cardiomyopathy and left ventricular non-compaction.
Presentation
De novo mutation rate in patients with hypertrophic cardiomyopathy and left ventricular non-compaction.
New insight into the clinical polymorphism of SCNA-related arrhythmic syndromes revealed by deep phenotyping
Presentation
New insight into the clinical polymorphism of SCNA-related arrhythmic syndromes revealed by deep phenotyping

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