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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Sparad:
Bibliografiska uppgifter
I publikationen:Front Cardiovasc Med
Huvudupphovsmän: Gourraud, Jean-Baptiste, Barc, Julien, Thollet, Aurélie, Le Scouarnec, Solena, Le Marec, Hervé, Schott, Jean-Jacques, Redon, Richard, Probst, Vincent
Materialtyp: Artigo
Språk:Inglês
Publicerad: Frontiers Media S.A. 2016
Ämnen:
Cardiovascular Medicine
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4842929/
https://ncbi.nlm.nih.gov/pubmed/27200363
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcvm.2016.00009
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