Novel SCN5A variants identified in a group of Iranian Brugada syndrome patients

Brugada syndrome (BrS) is a rare hereditary arrhythmia syndrome that increases an individual’s risk for sudden cardiac death (SCD) due to ventricular fibrillation. This disorder is regarded as a notable cause of death in individuals aged less than 40 years, responsible for up to 40% of sudden deaths...

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Veröffentlicht in:Functional & integrative genomics 2021-07, Vol.21 (3-4), p.331-340
Hauptverfasser: Ghaffari, Taraneh, Mirhosseini Motlagh, Naser, Daraei, Abdolreza, Tafrihi, Majid, Saravi, Mehrdad, Sabour, Davood
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Sprache:eng
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