QuickView for CACNA1D;jsessionid=6EBE27B2A80027D4CA2763981565EB84;jsessionid=8E18936F91C60677283EEE02138B97C8;jsessionid=3C6A40F2A1A9B2484D193E71C1BD037F;jsessionid=434DB03982826B90FCDA56B3E94EFDB8 (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 CACNA1D;jsessionid=6EBE27B2A80027D4CA2763981565EB84;jsessionid=8E18936F91C60677283EEE02138B97C8;jsessionid=3C6A40F2A1A9B2484D193E71C1BD037F;jsessionid=434DB03982826B90FCDA56B3E94EFDB8