Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block (Q33146611)

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Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block
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    Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block (English)

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