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Mutation in S6 domain of HCN4 channel in patient with suspected Brugada syndrome modifies channel function

Crossref DOI link: https://doi.org/10.1007/s00424-016-1870-1

Published Online: 2016-08-23

Published Print: 2016-10

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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