ESC Premium Access

Role of CACNA1C variants in Brugada syndrome: clinical aspects and genetic testing strategies

Session: Genetics
Topic: Genetics, Epigenetics, ncRNA

Congress Presentation

About the speaker

Doctor Valeria Novelli

Centro Cardiologico Monzino, Milan (Italy)
0 follower

6 more presentations in this session

Full-length-transcriptomic analysis in mice and human heart using Single-Molecule Real-time Sequencing (SMRT) identified 15 novel isoforms and a novel promoter region of PGC1-alpha

Speaker: Doctor D. Oehler (Duesseldorf, DE)

Thumbnail

Identification of six novel susceptibility loci for dyslipidemia by longitudinal exome-wide association studies in japanese

Speaker: Doctor M. Oguri (Kasugai, JP)

Thumbnail

A chromatin signature by the methyltransferase SETD7 regulates semaphorin-3G transcription and angiogenic response in diabetes: insights for personalized epigenetic therapies

Speaker: Mr S. Mohammed (Zurich, CH)

Thumbnail

Relationship between the expression level of genes of Ca(2+)-transporting proteins of the cardiomyocytes' sarcoplasmic reticulum with the severity of heart failure

Speaker: Miss E. Muslimova (Tomsk, RU)

Thumbnail

Epicardial adipose tissue: the genetics behind an emerging cardiovascular marker

Speaker: Doctor J. Sousa (Funchal, PT)

Thumbnail

Access the full session

Genetics

Speakers: Doctor V. Novelli, Doctor D. Oehler, Doctor M. Oguri, Mr S. Mohammed, Miss E. Muslimova...
Thumbnail

About the event

Image

ESC Congress 2020

29 August - 1 September 2020

Sessions Presentations

ESC 365 is supported by

logo Novo Nordisk
logo Bristol Myers Squibb