Atrial fibrillation, familial, 3
MONDO:0011857Any familial atrial fibrillation in which the cause of the disease is a mutation in the KCNQ1 gene.
Also known as: KCNQ1 familial atrial fibrillation, atrial fibrillation, familial, 3, atrial fibrillation, familial, type 3, familial atrial fibrillation caused by mutation in KCNQ1, ATFB3
30 clinical trials for this condition and its sub-types, 0 tagged with Atrial fibrillation, familial, 3 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.