Novel mutations in domain I of SCN5A cause Brugada syndrome.

M. Vatta, R. Dumaine, C. Antzelevitch, R. Brugada, H. Li, N.e. Bowles, K. Nademanee, J. Brugada, Pedro Brugada, J. Towbin

Research output: Contribution to journal › Article › peer-review

53 Citations (Scopus)

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Biochemistry, Genetics and Molecular Biology