A Novel Somatic Mutation of CACNA1H p.V1937M in Unilateral Primary Hyperaldosteronism

BackgroundSomatic mutations for excess aldosterone production have been frequently identified as important roles in the pathogenesis of unilateral primary hyperaldosteronism (uPA). Although CACNA1H mutation represents a minor etiology in primary aldosteronism, it plays a significant role in causing...

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Bibliographic Details
Main Authors: Chi-Shin Tseng, Kang-Yung Peng, Shuo-Meng Wang, Yao-Chou Tsai, Kuo-How Huang, Wei-Chou Lin, Ya-Hui Hu, Vin-Cent Wu, Jeff S. Chueh
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-06-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2022.816476/full

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