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QuickView for CACNA1D;jsessionid=0D3D2BF610EC14B3EF2AFF91B7A9648C (gene)
Most Relevant Literature
- CACNA1D-Related Channelopathies: From Hypertension to Autism.
- The human channel gating-modifying A749G CACNA1D (Cav1.3) variant induces a neurodevelopmental syndr…
- Germline de novo variant F747S extends the phenotypic spectrum of CACNA1D Ca2+ channelopathies.
- CACNA1D overexpression and voltage-gated calcium channels in prostate cancer during androgen depriva…
- Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with …
Most Relevant Clinical Trials
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