Cardiac conduction defects associate with mutations in SCN5A

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Figure 1: Pedigrees and symptoms of the PCCD families.
Figure 2: Identification of SCN5A mutations in the two families.

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Acknowledgements

We thank C. Fruchet and M.-J. Louërat for assistance and the families for participation. This work was supported by grants from the Institut National de la Santé et de la Recherche Médicale to H.L.M. and D.E. (PROGRES 4P009D); the Programme Hospitalier de Recherche Clinique (PHRC 1997) to H.L.M.; the Dutch Heart Foundation (NHS 95.014) to A.A.M.W; and the Inter-University Cardiology Institute, The Netherlands.

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Correspondence to Hervé Le Marec.

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Schott, J., Alshinawi, C., Kyndt, F. et al. Cardiac conduction defects associate with mutations in SCN5A. Nat Genet 23, 20–21 (1999) doi:10.1038/12618

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