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

206 clinical trials for this condition and its sub-types.

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