QuickView for CUL3;jsessionid=1D4498869E014023B15FD00DC9B4A28D;jsessionid=7F6CF583FDC17CEB1E2C8EED0FBAAB78;jsessionid=32EE5877698D2DAC23526195FD7F450D;jsessionid=4FD6BF927E06C6F75095F2AADAA51B7B;jsessionid=B5CBF409E0E3F56925A642BD90EA7981 (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=7F6CF583FDC17CEB1E2C8EED0FBAAB78;jsessionid=32EE5877698D2DAC23526195FD7F450D;jsessionid=4FD6BF927E06C6F75095F2AADAA51B7B;jsessionid=B5CBF409E0E3F56925A642BD90EA7981