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KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome

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Description scientific article
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author: Constantine A Stratakis  Anelia Horvath  Maria de la Luz Sierra  Monalisa Azevedo  Paraskevi Xekouki  Electron Kebebew  Dax Hoffman  Emmanouil Saloustros 

Publication date May 3, 2012
Language English
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