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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Bibliografski detalji
Izdano u:J Clin Endocrinol Metab
Glavni autori: 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
Jezik:Inglês
Izdano: Endocrine Society 2015
Teme:
JCEM Online: Advances in Genetics
Online pristup: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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