A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1
Clin Pediatr Endocrinol
.
2016 Oct;25(4):135-138.
doi: 10.1297/cpe.25.135.
Epub 2016 Oct 18.
Authors
Yoshimi Nishizaki
1
,
Makoto Hiura
2
,
Hidetoshi Sato
1
,
Yohei Ogawa
1
,
Akihiko Saitoh
1
,
Keisuke Nagasaki
1
Affiliations
1
Division of Pediatrics, Department of Homeostatic Regulation and Development, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
2
Department of Pediatrics, Kido Hospital, Niigata, Japan.
PMID:
27780983
PMCID:
PMC5069542
DOI:
10.1297/cpe.25.135
No abstract available
Keywords:
NR3C2; failure to thrive; mineralocorticoid receptor; pseudohypoaldosteronism type 1.