Cite
HARVARD Citation
Tanaka, T. et al. (2019). Complete clinical resolution of a Japanese family with renal pseudohypoaldosteronism type 1 due to a novel NR3C2 mutation. Nephrology. 24 (4), pp. 489-490. [Online].
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Tanaka, T. et al. (2019). Complete clinical resolution of a Japanese family with renal pseudohypoaldosteronism type 1 due to a novel NR3C2 mutation. Nephrology. 24 (4), pp. 489-490. [Online].