SCN5A mutation type and a genetic risk score associate variably with Brugada Syndrome Phenotype in SCN5A families - Wijeyeratne, Yanushi; Tanck, Michael W.; Mizusawa, Yuka; Batchvarov, Velislav; Barc, Julien; Crotti, Lia; Bos, J. Martijn; Tester, David J.; Muir, Alison; Veltmann, Christian; Ohno, Seiko; Page, Stephen P.; et al. (Circulation. Genomic and precision medicine, 2020)
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