Clinical Pediatric Endocrinology
Online ISSN : 1347-7358
Print ISSN : 0918-5739
ISSN-L : 0918-5739
Mutation-in-Brief
A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1
Yoshimi NishizakiMakoto HiuraHidetoshi SatoYohei OgawaAkihiko SaitohKeisuke Nagasaki
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2016 Volume 25 Issue 4 Pages 135-138

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© 2016 by The Japanese Society for Pediatric Endocrinology
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