CACNA1H Mutations Are Associated With Different Forms of Primary Aldosteronism

CACNA1H Mutations Are Associated With Different Forms of Primary Aldosteronism

Primary aldosteronism (PA) is the most common form of secondary hypertension. Mutations in KCNJ5, ATP1A1, ATP2B3 and CACNA1D are found in aldosterone producing adenoma (APA) and familial hyperaldosteronism (FH). A recurrent mutation in CACNA1H (coding for Cav3.2) was identified in a familial form of...

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Bibliographic Details
Main Authors: Georgios Daniil, Fabio L Fernandes-Rosa, Jean Chemin, Iulia Blesneac, Jacques Beltrand, Michel Polak, Xavier Jeunemaitre, Sheerazed Boulkroun, Laurence Amar, Tim M Strom, Philippe Lory, Maria-Christina Zennaro
Format: Article
Language:English
Published: Elsevier 2016-11-01
Series:EBioMedicine
Subjects:
Adrenal
Aldosterone producing adenoma
Familial hyperaldosteronism
Early onset hyperaldosteronism
Voltage dependent calcium channel
Hypertension
Online Access:http://www.sciencedirect.com/science/article/pii/S2352396416304571

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http://www.sciencedirect.com/science/article/pii/S2352396416304571

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