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Characteristics of a Novel ATP2B3 K416_F418delinsN Mutation in a Classical Aldosterone-Producing Adenoma

SIMPLE SUMMARY: The ATP2B3 channel mutation is a rare cause of primary aldosteronism (PA). ATP2B3 gene mutation leads to the dysfunction of calcium channel that pumps calcium ion out of the cell and accumulates intracellular calcium signal to stimulate aldosterone synthesis. In the present study, we...

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Detalles Bibliográficos
Autores principales:	Liao, Hung-Wei, Peng, Kang-Yung, Wu, Vin-Cent, Lin, Yen-Hung, Lin, Shuei-Liong, Lin, Wei-Chou, Chueh, Jeff S.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2021
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8472399/ https://www.ncbi.nlm.nih.gov/pubmed/34572956 http://dx.doi.org/10.3390/cancers13184729

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