A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1
Nishizaki, Yoshimi, Hiura, Makoto, Sato, Hidetoshi, Ogawa, Yohei, Saitoh, Akihiko, Nagasaki, Keisuke
Published in Clinical Pediatric Endocrinology (01.10.2016)
Published in Clinical Pediatric Endocrinology (01.10.2016)
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