QuickView for CACNA1D;jsessionid=5B69627D97B56DA68E561308D913ADF6;jsessionid=26FC2F01EC5838E809F0AE814A2413FE;jsessionid=E9E44038C6275F0E080EF8E1509CA0AA;jsessionid=18E0D74B66A89C0FF473966F0632C611 (gene)

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=5B69627D97B56DA68E561308D913ADF6;jsessionid=26FC2F01EC5838E809F0AE814A2413FE;jsessionid=E9E44038C6275F0E080EF8E1509CA0AA;jsessionid=18E0D74B66A89C0FF473966F0632C611