Analysis of a family with brugada syndrome and sudden cardiac death caused by a novel mutation of scn5a

HIGHLIGHTS

• who: Yao-Bin Zhu et al. from the Department of Traditional Chinese Medicine, The First Affiliated Hospital, Fujian Medical University, Fuzhou, China have published the research: Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A, in the Journal: Cardiology Research and Practice of 28/04/2022
• what: Detection of the SCN5A gene is helpful for the diagnosis of BrS, and the newly discovered SCN5A c.4313dup (p.Trp1439ValfsTer32) mutation enriches the mutation spectrum of the SCN5A gene.
• how: Three generations of a Chinese family . . .
  

   

  

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