ESC 365 - Mutations in RBM20 and titin cause left ventricular non-compaction cardiomyopathy

ESC Premium Access

Mutations in RBM20 and titin cause left ventricular non-compaction cardiomyopathy

Session: Best Posters 2 - Best Posters in genetics and gene therapy

Topic: Genetics and gene therapy

Speaker: Associate Professor F. Sedaghat-Hamedani (Heidelberg, DE)

Event: ESC Congress 2017

Congress Presentation

Add to my library

About the speaker

Associate Professor Farbod Sedaghat-Hamedani

University Hospital Heidelberg, Heidelberg (Germany)

1 presentation

0 follower

4 more presentations in this session

Discussant: Best Posters in genetics and gene therapy

Identification of 12q24.1, ACAD10, and BRAP as novel genetic determinants of blood pressure in Japanese individuals by exome-wide association studies

Speaker: Doctor H. Horibe (Tajimi, JP)

Trans-ethnic fine mapping of previously identified QT interval loci in han chinese discover ethnic-specific signals associated with inflammation pathway

Speaker: Professor J. Juang (Taipei, TW)

Hepatocyte-restricted SR-BI gene transfer corrects cardiac dysfunction in SR-BI deficient mice and improves pressure overload-induced cardiomyopathy

Speaker: Mr I. Muthuramu (Leuven, BE)

Access the full session

Best Posters 2 - Best Posters in genetics and gene therapy

Speakers: Associate Professor F. Sedaghat-Hamedani, Doctor H. Horibe, Professor J. Juang, Mr I. Muthuramu

About the event

ESC Congress 2017

26 August - 30 August 2017

Sessions Presentations

Congress

ESC 365 is supported by

Explore sponsored resources

Explore sponsored resources