Clinical Characteristics of SCN5A p.R965C Carriers: A Common Founder Variant Predisposing to Brugada Syndrome in Thailand

Circ Genom Precis Med. 2021 Jun;14(3):e003229. doi: 10.1161/CIRCGEN.120.003229. Epub 2021 Jun 7.
No abstract available

Keywords: Brugada syndrome; Thailand; gene frequency; phenotype; sodium channels; ventricular fibrillation.

Publication types

  • Clinical Trial
  • Letter
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Amino Acid Substitution
  • Brugada Syndrome / genetics*
  • Female
  • Genetic Testing
  • Humans
  • Male
  • Middle Aged
  • Mutation, Missense*
  • NAV1.5 Voltage-Gated Sodium Channel / genetics*
  • Thailand

Substances

  • NAV1.5 Voltage-Gated Sodium Channel
  • SCN5A protein, human

Associated data

  • ClinicalTrials.gov/NCT04232787