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Complete clinical resolution of a Japanese family with renal pseudohypoaldosteronism type 1 due to a novel NR3C2 mutation
Complete clinical resolution of a Japanese family with renal pseudohypoaldosteronism type 1 due to a novel NR3C2 mutation
2019
Tatsuhiko Tanaka
Eishin Oki
Takayasu Mori
Kazushi Tsuruga
Eisei Sohara
Shinichi Uchida
Hiroshi Tanaka
Keywords:
Diabetes mellitus
Intensive care medicine
Pediatrics
Medicine
Pseudohypoaldosteronism
Mutation
Correction
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