Molecular Genetics and Functional Anomalies in a Series of 248 Brugada Cases with 11 Mutations in the TRPM4 Channel

Brugada syndrome (BrS) is a condition defined by ST-segment alteration in right precordial leads and a risk of sudden death. Because BrS is often associated with right bundle branch block and the TRPM4 gene is involved in conduction blocks, we screened TRPM4 for anomalies in BrS cases. The DNA of 24...

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Detalles Bibliográficos
Autores principales: Liu, Hui, Chatel, Stéphanie, Simard, Christophe, Syam, Ninda, Salle, Laurent, Probst, Vincent, Morel, Julie, Millat, Gilles, Lopez, Michel, Abriel, Hugues, Schott, Jean-Jacques, Guinamard, Romain, Bouvagnet, Patrice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3559649/
https://www.ncbi.nlm.nih.gov/pubmed/23382873
http://dx.doi.org/10.1371/journal.pone.0054131

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3559649/
https://www.ncbi.nlm.nih.gov/pubmed/23382873
http://dx.doi.org/10.1371/journal.pone.0054131

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