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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Bibliografiske detaljer
Udgivet i:EBioMedicine
Main Authors: Daniil, Georgios, Fernandes-Rosa, Fabio L, Chemin, Jean, Blesneac, Iulia, Beltrand, Jacques, Polak, Michel, Jeunemaitre, Xavier, Boulkroun, Sheerazed, Amar, Laurence, Strom, Tim M, Lory, Philippe, Zennaro, Maria-Christina
Format: Artigo
Sprog:Inglês
Udgivet: Elsevier 2016
Fag:
Research Paper
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5264314/
https://ncbi.nlm.nih.gov/pubmed/27729216
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ebiom.2016.10.002
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