Associated Papers
Cardiac sodium channel overlap syndromes: different faces of SCN5A mutations.
Remme CA et al.
Trends in Cardiovascular Medicine, 2008
[Homozygotous mutation of the SCN5A gene responsible for congenital long QT syndrome with 2/1 atrioventricular block].
Lupoglazoff JM et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux, 2002
Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block.
Lupoglazoff JM et al.
Circulation Research, 2001
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