Identification of a new SCN5A mutation, D1840G, associated with the long QT syndrome. Mutations in brief no. 153. Online.

J. Benhorin, M. Goldmit, J. W. MacCluer, J. Blangero, R. Goffen, A. Leibovitch, A. Rahat, Q. Wang, A. Medina, J. Towbin, B. Kerem

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