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Long-read sequence confirmed a large deletion of MYH6 and MYH7 in a family with atrial septal defect

29 August 2020 (00:00 - 00:00)
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Congress Presentation Part of: Basic Science Cardiac ePosters Congenital Heart Disease ESC Premium Access ESC Congress 2020

About the speaker

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Doctor Keiko Sonoda

National Cerebral & Cardiovascular Center, Suita (Japan)

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Single-cell RNA sequencing of human fetal epicardium reveals novel markers and regulators of EMT
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Genome-wide association study identifies 18 new susceptibility variants loci associated with Brugada Syndrome
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Mutations in CHMP4C cause dilated cardiomyopathy via dysregulation of autophagy
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Disruption of the architecture of the junctional sarcoplasmic reticulum in recessive catecholaminergic polymorphic ventricular tachycardia is caused by the er-shaping proteins reep5 and climp63
Doctor R. Bongianino (Pavia, IT)
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Access the full session

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Basic Science Cardiac ePosters

The Event

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ESC Congress 2020

29 August - 1 September 2020
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