Cardiac conduction defects associate with mutations in SCN5A.
Schott JJ; Alshinawi C; Kyndt F; Probst V; Hoorntje TM; Hulsbeek M; Wilde AA; Escande D; Mannens MM; Le Marec H; Nature Genetics, 1999, vol. 23, issue 1, p 20, ISSN 10614036. ISBN 10614036.

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