QuickView for CUL3;jsessionid=1D4498869E014023B15FD00DC9B4A28D;jsessionid=7F6CF583FDC17CEB1E2C8EED0FBAAB78;jsessionid=32EE5877698D2DAC23526195FD7F450D;jsessionid=35B49469D375B1C10090841C6A30E538 (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=7F6CF583FDC17CEB1E2C8EED0FBAAB78;jsessionid=32EE5877698D2DAC23526195FD7F450D;jsessionid=35B49469D375B1C10090841C6A30E538