Associated Papers
New mutation of CACNA1H p.Tyr613Phe in hyperaldosteronism: a case report.
Yan Q et al.
Frontiers in Medicine, 2025
Genetic variants and down-regulation of CACNA1H in pheochromocytoma.
Svahn F et al.
Endocrine-related Cancer, 2024
Primary aldosteronism: molecular medicine meets public health.
Azizan EAB et al.
Nature Reviews. Nephrology, 2023
CaV3.2 (CACNA1H) in Primary Aldosteronism.
Dinh HA et al.
Handbook of Experimental Pharmacology, 2023
Customised targeted massively parallel sequencing enables more precise diagnosis of patients with epilepsy.
Atli EI et al.
Internal Medicine Journal, 2022
A Novel Somatic Mutation of CACNA1H p.V1937M in Unilateral Primary Hyperaldosteronism.
Tseng CS et al.
Frontiers in Endocrinology, 2022
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