Primary Aldosteronism and ARMC5 Variants

CONTEXT: Primary aldosteronism is one of the leading causes of secondary hypertension, causing significant morbidity and mortality. A number of genetic defects have recently been identified in primary aldosteronism, whereas we identified mutations in ARMC5, a tumor-suppressor gene, in cortisol-produ...

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Veröffentlicht in:J Clin Endocrinol Metab
Hauptverfasser: Zilbermint, Mihail, Xekouki, Paraskevi, Faucz, Fabio R., Berthon, Annabel, Gkourogianni, Alexandra, Schernthaner-Reiter, Marie Helene, Batsis, Maria, Sinaii, Ninet, Quezado, Martha M., Merino, Maria, Hodes, Aaron, Abraham, Smita B., Libé, Rossella, Assié, Guillaume, Espiard, Stéphanie, Drougat, Ludivine, Ragazzon, Bruno, Davis, Adam, Gebreab, Samson Y., Neff, Ryan, Kebebew, Electron, Bertherat, Jérôme, Lodish, Maya B., Stratakis, Constantine A.
Format: Artigo
Sprache:Inglês
Veröffentlicht: Endocrine Society 2015
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JCEM Online: Advances in Genetics
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4454793/
https://ncbi.nlm.nih.gov/pubmed/25822102
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2014-4167
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