Publication | Open Access
Novel <i>KLHL26</i> variant associated with a familial case of Ebstein’s anomaly and left ventricular noncompaction
16
Citations
46
References
2020
Year
In this familial case of EA/LVNC, we have identified a candidate gene variant, KLHL26 (p.R237C), which may have an important role in ubiquitin-mediated protein degradation during cardiac development.
| Year | Citations | |
|---|---|---|
Page 1
Page 1