A novel mutation in the human mineralocorticoid receptor gene in a Japanese          family with autosomal-dominant pseudohypoaldosteronism type 1

Mutation-in-Brief

A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1

Author information

Yoshimi Nishizaki
Division of Pediatrics, Department of Homeostatic Regulation and Development, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan
Makoto Hiura
Department of Pediatrics, Kido Hospital, Niigata, Japan
Hidetoshi Sato
Division of Pediatrics, Department of Homeostatic Regulation and Development, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan
Yohei Ogawa
Division of Pediatrics, Department of Homeostatic Regulation and Development, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan
Akihiko Saitoh
Division of Pediatrics, Department of Homeostatic Regulation and Development, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan
Keisuke Nagasaki
Division of Pediatrics, Department of Homeostatic Regulation and Development, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan

JOURNAL OPEN ACCESS

2016 Volume 25 Issue 4 Pages 135-138

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