BÉBAROVÁ, Markéta, RJ JONGBLOED, C TIMMERMANS, YH ARENS, PGA VOLDERS and LM RODRIGUEZ. Four Novel Mutations in Patients with Brugada Syndrome. In The 29th meeting of the European Working Group of Cardiac Cellular Electrophysiology, Antwerp (Belgium), 9. – 11. 9. 2005. 2005.
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Basic information
Original name Four Novel Mutations in Patients with Brugada Syndrome
Authors BÉBAROVÁ, Markéta, RJ JONGBLOED, C TIMMERMANS, YH ARENS, PGA VOLDERS and LM RODRIGUEZ.
Edition The 29th meeting of the European Working Group of Cardiac Cellular Electrophysiology, Antwerp (Belgium), 9. – 11. 9. 2005, 2005.
Other information
Original language English
Type of outcome Presentations at conferences
Field of Study 30201 Cardiac and Cardiovascular systems
Country of publisher Belgium
Confidentiality degree is not subject to a state or trade secret
Organization unit Faculty of Medicine
Keywords in English Brugada syndrome; mutation; genetic analysis
Tags International impact
Changed by Changed by: doc. MUDr. Markéta Bébarová, Ph.D., učo 15000. Changed: 26/4/2011 14:12.
Abstract
We identified four novel SCN5A mutations in patients with BrS out of eighteen patients tested (22% novel positive identification). A mutation in an untranslated region of the SCN5A gene is recognized, which correlates with a severe clinical phenotype. Thus, our data stress the importance of genetic testing of noncoding regions in BrS.
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