Mini Symposium How genetics can identify genes/pathways implied in cardiac diseases

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  • Le 18 décembre 2018
    Institut de Recherche en Santé - 8 quai Moncousu - Nantes
    Amphithéâtre Denis Escande
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  • 09h45 - 12h15

How genetics can identify genes/pathways implied in cardiac diseases

  • 09H45 – 10H15              

Charlotte Glinge - Department of Cardiology, Rigshospitalet, Copenhagen, Danemark

Meta-Analysis of Genome Wide Association Studies of Ventricular Fibrillation during first acute Myocardial Infarction

  • 10H15 - 10H45             

Rafik TADROS - Montreal Heart Institute, Canada

Genome-wide association study in hypertrophic cardiomyopathy provides novel insights on disease mechanism

  • 10H45 – 11H30

Connie BEZZINA - Department of Clinical and Experimental Cardiology, Amsterdam, Pays-Bas

Genome-wide association study in probands with Long QT Syndrome

  • 11H30 – 12H15               

Naomasa MAKITA - Department of Molecular Physiology, Nagasaki, Japon

Cardiac Emerinopathy, Novel Non-syndromic X-linked Left Ventricular Noncompaction Associated with Progressive Atrial Conduction Disturbance

Mis à jour le 31 décembre 2018.
https://umr1087.univ-nantes.fr/home/events/mini-symposium-how-genetics-can-identify-genes-pathways-implied-in-cardiac-diseases