QuickView for CUL3;jsessionid=E34D267D0C8AB0024346F7214B5B73A3 (gene)

1. Insights into the diverse mechanisms and effects of variant CUL3-induced familial hyperkalemic hyper…
2. Are CUL3 variants an underreported cause of congenital heart disease?
3. Renal effects of cullin 3 mutations causing familial hyperkalemic hypertension.
4. A novel splice site CUL3 variant in a patient with neurodevelopmental delay.
5. Structure and Function of RhoBTB1 Required for Substrate Specificity and Cullin-3 Ubiquitination.

There were no clinical trials for CUL3;jsessionid=E34D267D0C8AB0024346F7214B5B73A3