Population
Patients with atrial septal defect and associated electrical disorders or genetic mutations
Design
Review
Authors
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May support genetic evaluation in ASD with conduction defects; leaves open prospective validation of SCD risk.
This review highlights the genetic basis of inherited atrial septal defects associated with cardiac conduction disorders, specifically TBX5 and NKX2-5 mutations.
Aoki et al. (2018) studied this question.
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