QuickView for NM_001257197 (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 NM_001257197