From genotype to phenotype: Clinical assessment and participant perspective of a secondary genomic finding associated with long QT syndrome
Genomic variants associated with inherited cardiac conditions (ICC) yet detected incidentally (secondary findings [SF]) are likely to arise with increasing frequency as genome sequencing (GS) transitions into clinical practice. Because genotyping has until recently been directed by clinical diagnosi...
| Main Authors: | , , , , |
|---|---|
| Format: | Journal article |
| Published: |
American Heart Association
2018
|