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, KeisukeVolume:
25
Year:
2016
Language:
english
Journal:
Clinical Pediatric Endocrinology
DOI:
10.1297/cpe.25.135
File:
PDF, 1.07 MB
english, 2016