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Scott J.J., Alshinawi C., Kyndt F., Probst V., Hoorntje T.M., Hulsbeek M., Wilde A.A.M., Escande D., Mannens M.M.A.M., Le Marec H. Cardiac conduction defect associate with mutations in SCN5A. - Nature Genet., 1999, v. 23, p. 20-21.
