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Compound Heterozygous SCN5A Mutations in Severe Sodium Channelopathy with Brugada Syndrome: A Case Report.

Aleksandra Nijak,Alain J. Labro,Hans De Wilde,Wendy Dewals,Steve Peigneur,Jan Tytgat,Dirk Snyders,Ewa Sieliwonczyk,Eline Simons,Emeline Van Craenenbroeck,Dorien Schepers,Lut Van Laer,Johan Saenen,Bart Loeys,Maaike Alaerts

Frontiers in Cardiovascular Medicine（2020）

Cited 4|Views0
Key words
Brugada syndrome,cardiac arrhythmia,SCN5A,case report,compound heterozygosity
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