Project information
Project information
Výskyt polymorfizmů genů pro iontové kanály myokardu ve vztahu k náhlé srdeční smrti u pacientů se strukturálním onemocněním srdce
- Project Identification
- NR9340
- Project Period
- 1/2007 - 12/2009
- Investor / Pogramme / Project type
-
Ministry of Health of the CR
- Ministry of Agriculture R&D Programme
- MU Faculty or unit
- Faculty of Medicine
- Cooperating Organization
-
University Hospital Brno-Bohunice
- Responsible person prof. MUDr. Tomáš Novotný, Ph.D.
Publications
Total number of publications: 3
2011
-
Mutation Analysis Ion Channel Genes Ventricular Fibrillation Survivors with Coronary Artery Disease
PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY, year: 2011, volume: 34, edition: 6, DOI
2010
-
A new homozygous mutation of the KCNQ1 gene associated with both Romano-Ward and incomplete Jervell Lange-Nielsen syndromes in two sisters
Heart Rhythm, year: 2010, volume: 7, edition: 4, DOI
2008
-
Mutation analysis of candidate genes SCN1B, KCND3 and ANK2 in patients with clinical diagnosis of Long QT syndrome.
Physiological Research, year: 2008, volume: 57/2008, edition: 6