QuickView for CACNA1D;jsessionid=2A340C388FA59F40E4185E4CF05634CA;jsessionid=B17E34CEF8D378E3CFC0249C2C2AD8D3;jsessionid=211E249F9DC322880AF1BB605190538D;jsessionid=956D5E7A701D5F62F4F07CCC6E6DF8D4;jsessionid=80EE7A93FC27BA77EDE21D19F9F23066 (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=2A340C388FA59F40E4185E4CF05634CA;jsessionid=B17E34CEF8D378E3CFC0249C2C2AD8D3;jsessionid=211E249F9DC322880AF1BB605190538D;jsessionid=956D5E7A701D5F62F4F07CCC6E6DF8D4;jsessionid=80EE7A93FC27BA77EDE21D19F9F23066