QuickView for CUL3;jsessionid=1D4498869E014023B15FD00DC9B4A28D;jsessionid=FF2BDA1A2FE9863E66551CCB12D49E92;jsessionid=600C69E4D80165A83C84964249A07FAE;jsessionid=DC8213A83036EB77D97D78E95F57B847 (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=1D4498869E014023B15FD00DC9B4A28D;jsessionid=FF2BDA1A2FE9863E66551CCB12D49E92;jsessionid=600C69E4D80165A83C84964249A07FAE;jsessionid=DC8213A83036EB77D97D78E95F57B847