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- W8930798 abstract "Three new heterozygous mutations were detected in patients with Brugada syndrome in SCN5A gene coding the alpha-subunit of sodium channel, two of them frameshift mutations with complete loss of function and one missense mutation with decreased sodium current and impaired inactivation gating." @default.
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- W8930798 date "2006-01-01" @default.
- W8930798 modified "2023-09-26" @default.
- W8930798 title "Functional defect of three novel SCN5A mutations in patients with Brugada syndrome" @default.
- W8930798 hasPublicationYear "2006" @default.
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