QuickView for CUL3;jsessionid=1D4498869E014023B15FD00DC9B4A28D;jsessionid=D79A5630D4DBD41B67EA6BA7D093D2B7;jsessionid=0259127A1542ED3F6DA0D1C31399B868;jsessionid=0FCC2CFAD4BA6985303E3178AF868CD9 (gene)

1. Renal effects of cullin 3 mutations causing familial hyperkalemic hypertension.
2. A novel splice site CUL3 variant in a patient with neurodevelopmental delay.
3. Structure and Function of RhoBTB1 Required for Substrate Specificity and Cullin-3 Ubiquitination.
4. A case of novel mutation of Cullin 3 gene in pseudohypoaldosteronism type II.
5. The Role of Cullin 3 in Cerebral Ischemia-Reperfusion Injury.

There were no clinical trials for CUL3;jsessionid=1D4498869E014023B15FD00DC9B4A28D;jsessionid=D79A5630D4DBD41B67EA6BA7D093D2B7;jsessionid=0259127A1542ED3F6DA0D1C31399B868;jsessionid=0FCC2CFAD4BA6985303E3178AF868CD9