QuickView for NM_001128840 (gene)

1. CACNA1D-Related Channelopathies: From Hypertension to Autism.
2. Germline de novo variant F747S extends the phenotypic spectrum of CACNA1D Ca2+ channelopathies.
3. CACNA1D overexpression and voltage-gated calcium channels in prostate cancer during androgen depriva…
4. Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with …
5. Dominant role of CACNA1D exon mutations for blood pressure regulation.

There were no clinical trials for NM_001128840