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Filters: Author is Violleau, Jade [Clear All Filters]
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2016. Dysfunction of the Voltage‐Gated K $^\textrm+}$ Channel β2 Subunit in a Familial Case of Brugada Syndrome. Journal of the American Heart Association. 5
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2015. Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome. Human Molecular Genetics. 24:2757–2763.
