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An infantile case of pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation of NR3C2
An infantile case of pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation of NR3C2
2020
Takeshi Goda
Hiroshi Komatsu
Kandai Nozu
Hisakazu Nakajima
Keywords:
Medicine
Diabetes mellitus
Endocrinology
Internal medicine
Pseudohypoaldosteronism
novel mutation
Correction
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