Brugada syndrome 7

MONDO:0013146

Any Brugada syndrome in which the cause of the disease is a mutation in the SCN3B gene.

Also known as: BRGDA7, Brugada syndrome 7, Brugada syndrome caused by mutation in SCN3B, Brugada syndrome type 7, SCN3B Brugada syndrome, atrial fibrillation, familial, 16

32 clinical trials for this condition and its sub-types, 0 tagged with Brugada syndrome 7 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Brugada syndrome (10)

Including sub-types (32) Tagged with Brugada syndrome 7 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.