A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease (Q84445454)

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scientific article published on 01 August 2010
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A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease
scientific article published on 01 August 2010

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    A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease (English)

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