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Dive into the research topics of 'A novel Y152C KCNJ5 mutation responsible for familial hyperaldosteronism type III'. Together they form a unique fingerprint.- Sort by
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Silvia Monticone, Namita G. Hattangady, David Penton, Carlos M. Isales, Michael A. Edwards, Tracy A. Williams, Christina Sterner, Richard Warth, Paolo Mulatero, William E. Rainey
Research output: Contribution to journal › Article › peer-review