Back
ESC Premium Access

Risk and prognosis of mutations in different regions of the KCNQ1 gene.

Session: Genetic basis
Topic: Genetic aspects of arrhythmias
Speaker: Doctor M. Cicerchia (Espoo, FI)
Event: ESC Congress 2017

Congress Presentation

Add to my library

Like

About the speaker

Doctor Marcos Nicolas Cicerchia

Blueprint Genetics, a Quest Diagnostics Company, Espoo (Finland)
0 follower

6 more presentations in this session

Identification of genetic etiology of malignant arrhythmia in dilated cardiomyopathy.

Speaker: Doctor D. Wang (Nanjing, CN)

Access
Abstract
Like
Thumbnail

Study of pharmacodynamic and pharmacokinetic-mediated genetic susceptibility to drug-induced arrhythmia and sudden cardiac death

Speaker: Miss M. Martinez Matilla (Santiago de Compostela, ES)

Access
Abstract
Slides
Like
Thumbnail

Genotype-phenotype correlation of novel KV7.1 mutations identified in patients with Long QT syndrome

Speaker: Doctor M. Refaat (Beirut, LB)

Access
Abstract
Slides
Like
Thumbnail

Novel RYR2 mutations causative for long QT syndromes

Speaker: Doctor M. Fukuyama (Otsu, JP)

Access
Abstract
Slides
Like
Thumbnail

High frequency of CACNA1C mutations among genotyped LQTS patients

Speaker: Assistant Professor S. Ohno (Suita, JP)

Access
Abstract
Slides
Like
Thumbnail

Access the full session

Genetic basis

Speakers: Doctor M. Cicerchia, Doctor D. Wang, Miss M. Martinez Matilla, Doctor M. Refaat, Doctor M. Fukuyama...
Access
Like
Thumbnail

About the event

Image

ESC Congress 2017

26 August - 30 August 2017

Sessions Presentations

Congress
logo Image

ESC 365 is supported by

logo Bristol Myers Squibb Explore sponsored resources
logo Novo Nordisk Explore sponsored resources