QuickView for CACNA1D;jsessionid=3F6D378662A2C4C6F2B59F59107A376F;jsessionid=15BA4C9C83AF08E79EE9EDB13B44E1B2;jsessionid=BFCD8BDC0D52D456E3A403D79FBB747A;jsessionid=6F902E6C88A2D0ADA43703CDF6132E9E;jsessionid=1469089280B014655B7EBD9C90DD2078 (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=3F6D378662A2C4C6F2B59F59107A376F;jsessionid=15BA4C9C83AF08E79EE9EDB13B44E1B2;jsessionid=BFCD8BDC0D52D456E3A403D79FBB747A;jsessionid=6F902E6C88A2D0ADA43703CDF6132E9E;jsessionid=1469089280B014655B7EBD9C90DD2078