QuickView for XM_011534097;jsessionid=BA56AA58AE2542889A2DA497C63230DA;jsessionid=D37E9F9804E53DE6A0C6CF7F7CF3E7CE;jsessionid=D907EF7167E6A709946A5F5C980DCA9C (gene)

1. CaV1.3 channel clusters characterized by live-cell and isolated plasma membrane nanoscopy.
2. Undiagnosed Disease Network collaborative approach in diagnosing rare disease in a patient with a mo…
3. CACNA1D-Related Channelopathies: From Hypertension to Autism.
4. The human channel gating-modifying A749G CACNA1D (Cav1.3) variant induces a neurodevelopmental syndr…
5. Germline de novo variant F747S extends the phenotypic spectrum of CACNA1D Ca2+ channelopathies.

There were no clinical trials for XM_011534097;jsessionid=BA56AA58AE2542889A2DA497C63230DA;jsessionid=D37E9F9804E53DE6A0C6CF7F7CF3E7CE;jsessionid=D907EF7167E6A709946A5F5C980DCA9C