QuickView for CACNA1D;jsessionid=DB663231A3FE3DAE7A6DADF8A2B0EA66;jsessionid=475E9C7635CF4774B8C71F6D5C15BC4E;jsessionid=BDC8BECFC96484E4281372ECD96361B6;jsessionid=FC84BC13CE85B2DC1B305F3F1270F784;jsessionid=DAD86CE7BB34C1B5C829CECCC216AC70;jsessionid=4D7F036B6A930E8D85DC4D79ED7E5CBD;jsessionid=DD39399C524FB4CCE292946379D0BC50;jsessionid=AF26D51C5CD6181D730C3659BE8AFA54 (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 CACNA1D;jsessionid=DB663231A3FE3DAE7A6DADF8A2B0EA66;jsessionid=475E9C7635CF4774B8C71F6D5C15BC4E;jsessionid=BDC8BECFC96484E4281372ECD96361B6;jsessionid=FC84BC13CE85B2DC1B305F3F1270F784;jsessionid=DAD86CE7BB34C1B5C829CECCC216AC70;jsessionid=4D7F036B6A930E8D85DC4D79ED7E5CBD;jsessionid=DD39399C524FB4CCE292946379D0BC50;jsessionid=AF26D51C5CD6181D730C3659BE8AFA54