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The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance

For the last 10 years, applying new sequencing technologies to thousands of whole exomes has revealed the high variability of the human genome. Extreme caution should thus be taken to avoid misinterpretation when associating rare genetic variants to disease susceptibility. The Brugada syndrome (BrS)...

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Detalles Bibliográficos
Autores principales: Gourraud, Jean-Baptiste, Barc, Julien, Thollet, Aurélie, Le Scouarnec, Solena, Le Marec, Hervé, Schott, Jean-Jacques, Redon, Richard, Probst, Vincent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4842929/
https://www.ncbi.nlm.nih.gov/pubmed/27200363
http://dx.doi.org/10.3389/fcvm.2016.00009