Embryonic type Na+ channel β-subunit, SCN3B masks the disease phenotype of Brugada syndrome
SCN5A is abundant in heart and has a major role in I Na . Loss-of-function mutation in SCN5A results in Brugada syndrome (BrS), which causes sudden death in adults. It remains unclear why disease phenotype does not manifest in the young even though mutated SCN5A is expressed in the young. The aim of...
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Veröffentlicht in: | Scientific reports 2016-09, Vol.6 (1), p.34198-34198, Article 34198 |
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Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Sprache: | eng |
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