Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A gene

Lignende værker

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  af: Krogh Broendberg, Anders, et al.
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  af: Broendberg, Anders Krogh, et al.
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• A Novel SCN5A Mutation in a Patient with Coexistence of Brugada Syndrome Traits and Ischaemic Heart Disease
  af: Holst, Anders G., et al.
  Udgivet: (2009)
• Failure of ICD therapy in lethal arrhythmogenic right ventricular cardiomyopathy type 5 caused by the TMEM43 p.Ser358Leu mutation
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  Udgivet: (2016)