Pseudohypoaldosteronism Type 1 with a Novel Mutation in the NR3C2 Gene: A Case Report
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Child Kidney Dis. 2020;24(1):58-61.   Published online 2020 Apr 30     DOI:
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A Neonate with Autosomal Dominant Pseudohypoaldosteronism Type 1 Due to a Novel Microdeletion of the NR3C2 Gene at 4q31.23
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