Novel SCN5A mutations in two families with “Brugada-like” ST elevation in the inferior leads and conduction disturbances-Reference-Cited by-同舟云学术

Novel SCN5A mutations in two families with “Brugada-like” ST elevation in the inferior leads and conduction disturbances

Published:2013-04-24 Issue:2 Volume:37 Page:131-140
ISSN:1383-875X
Container-title:Journal of Interventional Cardiac Electrophysiology
language:en
Short-container-title:J Interv Card Electrophysiol

Author:

Maury Philippe,Moreau Adrien,Hidden-Lucet Francoise,Leenhardt Antoine,Fressart Veronique,Berthet Myriam,Denjoy Isabelle,Bennamar Nawal,Rollin Anne,Cardin Christelle,Guicheney Pascale,Chahine Mohamed

Publisher

Springer Science and Business Media LLC

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Link

http://link.springer.com/content/pdf/10.1007/s10840-013-9805-7.pdf

Reference38 articles.

1. Antzelevitch, C., Brugada, P., Borggrefe, M., Brugada, J., Brugada, R., Corrado, D., et al. (2005). Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association. Circulation, 111, 659–670.

2. Potet, F., Mabo, P., Le Coq, G., Probst, V., Schott, J. J., Airaud, F., et al. (2003). Novel brugada SCN5A mutation leading to ST segment elevation in the inferior or the right precordial leads. Journal of Cardiovascular Electrophysiology, 14, 200–203.

3. Riera, A. R., Ferreira, C., Schapachnik, E., Sanches, P. C., & Moffa, P. J. (2004). Brugada syndrome with atypical ECG: downsloping ST-segment elevation in inferior leads. J Electrocardiol, 37, 101–104.

4. Lombardi, F., Potenza, S., Beltrami, A., Verzoni, A., Brugada, P., & Brugada, R. (2007). Simultaneous ST-segment elevation in the right precordial and inferior leads in Brugada syndrome. Journal of Cardiovascular Medicine (Hagerstown, Md.), 8, 201–204.

5. Van den Berg, M. P., & Wiesfeld, A. C. (2006). Brugada syndrome with ST-segment elevation in the lateral leads. Journal of Cardiovascular Electrophysiology, 17, 1035.

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Evaluating the Use of Genetics in Brugada Syndrome Risk Stratification;Frontiers in Cardiovascular Medicine;2021-04-21

2. Novel SCN5A variants identified in a group of Iranian Brugada syndrome patients;Functional & Integrative Genomics;2021-02-27

3. Pathological turret mutations in the cardiac sodium channel cause long-range pore disruption;2021-01-17

4. Genotype–Phenotype Correlation in a Family with Brugada Syndrome Harboring the Novel p.Gln371* Nonsense Variant in the SCN5A Gene;International Journal of Molecular Sciences;2019-11-06

5. Novel SCN5A p.W697X Nonsense Mutation Segregation in a Family with Brugada Syndrome;International Journal of Molecular Sciences;2019-10-04