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An infantile case of pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation of NR3C2.

ABSTRACT:

SUBMITTER: Goda T 

PROVIDER: S-EPMC7348633 | biostudies-literature | 2020

REPOSITORIES: biostudies-literature

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An infantile case of pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation of <i>NR3C2</i>.

Goda Takeshi T   Komatsu Hiroshi H   Nozu Kandai K   Nakajima Hisakazu H  

Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology 20200711 3

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