QuickView for CACNA1D;jsessionid=2A340C388FA59F40E4185E4CF05634CA;jsessionid=B17E34CEF8D378E3CFC0249C2C2AD8D3 (gene)

No studies found

1. CACNA1D-Related Channelopathies: From Hypertension to Autism.
2. The human channel gating-modifying A749G CACNA1D (Cav1.3) variant induces a neurodevelopmental syndr…
3. Germline de novo variant F747S extends the phenotypic spectrum of CACNA1D Ca2+ channelopathies.
4. CACNA1D overexpression and voltage-gated calcium channels in prostate cancer during androgen depriva…
5. Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with …

There were no clinical trials for CACNA1D;jsessionid=2A340C388FA59F40E4185E4CF05634CA;jsessionid=B17E34CEF8D378E3CFC0249C2C2AD8D3