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

BACKGROUND: Somatic 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 causin...

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Detalles Bibliográficos
Autores principales:	Tseng, Chi-Shin, Peng, Kang-Yung, Wang, Shuo-Meng, Tsai, Yao-Chou, Huang, Kuo-How, Lin, Wei-Chou, Hu, Ya-Hui, Wu, Vin-Cent, Chueh, Jeff S.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2022
Materias:	Endocrinology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218183/ https://www.ncbi.nlm.nih.gov/pubmed/35757409 http://dx.doi.org/10.3389/fendo.2022.816476

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