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The many faces of SCN5A pathogenic variants: from channelopathy to cardiomyopathy.
SCN5A gene variants and arrhythmic risk in Brugada syndrome: An updated systematic review and meta-a…
A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in…
SCN5A channelopathy: arrhythmia, cardiomyopathy, epilepsy and beyond.
Functional characterization of QT interval associated SCN5A enhancer variants identify combined addi…
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IDOMENEO - Is Treatment Reality in Vascular Medicine Evidence-based and Follows Guideline Recommenda…
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